geneid | 4057 |
---|---|
ensemblid | ENSG00000012223.13 |
hgncid | 6720 |
symbol | LTF |
name | lactotransferrin |
refseq_nuc | NM_002343.6 |
refseq_prot | NP_002334.2 |
ensembl_nuc | ENST00000231751.9 |
ensembl_prot | ENSP00000231751.4 |
mane_status | MANE Select |
chr | chr3 |
start | 46435645 |
end | 46464905 |
strand | - |
ver | v1.2 |
region | chr3:46435645-46464905 |
region5000 | chr3:46430645-46469905 |
regionname0 | LTF_chr3_46435645_46464905 |
regionname5000 | LTF_chr3_46430645_46469905 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 711 | 174 | 51 | 31 | 69 | 6 | 17 | 51 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002 | 0/1 | 711 | 74 | 2 | 20 | 43 | 2 | 6 | 41 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003 | 0/0 | 711 | 45 | 2 | 10 | 19 | 6 | 8 | 16 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004 | 0/0 | 711 | 38 | 11 | 6 | 14 | 0 | 7 | 11 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0005 | 0/0 | 711 | 35 | 0 | 0 | 34 | 0 | 1 | 27 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006 | 0/0 | 711 | 23 | 1 | 4 | 16 | 1 | 1 | 9 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0007 | 0/0 | 711 | 17 | 16 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0008 | 0/0 | 711 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0009 | 0/0 | 711 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0010 | 1/0 | 710 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0011 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0012 | 0/0 | 711 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0013 | 0/0 | 711 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0014 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0015 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0016 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0017 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0018 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0019 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0020 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0021 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0022 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0023 | 0/0 | 711 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0024 | 0/0 | 711 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2136 | 75 | 14 | 9 | 39 | 6 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0002 | 0/0 | 2136 | 57 | 9 | 12 | 27 | 0 | 9 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0003 | 0/0 | 2136 | 49 | 0 | 4 | 42 | 0 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0004 | 0/0 | 2136 | 43 | 2 | 10 | 18 | 6 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0005 | 0/0 | 2136 | 33 | 0 | 0 | 32 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0006 | 0/1 | 2136 | 23 | 1 | 16 | 0 | 2 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0007 | 0/0 | 2136 | 19 | 17 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0008 | 0/0 | 2136 | 17 | 16 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0009 | 0/0 | 2136 | 12 | 0 | 0 | 12 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0010 | 0/0 | 2136 | 12 | 0 | 5 | 0 | 0 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0011 | 0/0 | 2136 | 9 | 1 | 5 | 2 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0012 | 0/0 | 2136 | 8 | 0 | 0 | 8 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0013 | 0/0 | 2136 | 5 | 0 | 3 | 1 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0014 | 0/0 | 2136 | 5 | 3 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0015 | 0/0 | 2136 | 5 | 4 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0016 | 0/0 | 2136 | 5 | 0 | 0 | 5 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0017 | 0/0 | 2136 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0018 | 0/0 | 2136 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0019 | 0/0 | 2136 | 2 | 1 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0020 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0021 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0022 | 0/0 | 2136 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0023 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0024 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0025 | 0/0 | 2136 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0026 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0027 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0028 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0029 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0030 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0031 | 0/0 | 2136 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0032 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0033 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0034 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0035 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0036 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0037 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0038 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0039 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0040 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0041 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0042 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0043 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0044 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0045 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0046 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0047 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0048 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0049 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0050 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0051 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0052 | 0/0 | 2133 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0053 | 1/0 | 2133 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0054 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0055 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
c0056 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 589 | 289 | 79 | 58 | 112 | 9 | 29 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
t0002 | 0/0 | 589 | 105 | 4 | 14 | 69 | 7 | 11 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
t0003 | 0/0 | 589 | 30 | 8 | 0 | 21 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
t0004 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
t0005 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
t0006 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
t0007 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0002 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0003 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0004 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0006 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0008 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0015 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0038 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0056 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0057 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0060 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2136 | 75 | 14 | 9 | 39 | 6 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0002 | 0/0 | 2136 | 57 | 9 | 12 | 27 | 0 | 9 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0007 | 0/0 | 2136 | 19 | 17 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0011 | 0/0 | 2136 | 9 | 1 | 5 | 2 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0014 | 0/0 | 2136 | 5 | 3 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0019 | 0/0 | 2136 | 2 | 1 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0020 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0021 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0030 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0034 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0054 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0003 | 0/0 | 2136 | 49 | 0 | 4 | 42 | 0 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0006 | 0/1 | 2136 | 23 | 1 | 16 | 0 | 2 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0036 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0042 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0004 | 0/0 | 2136 | 43 | 2 | 10 | 18 | 6 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0038 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0041 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0010 | 0/0 | 2136 | 12 | 0 | 5 | 0 | 0 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0012 | 0/0 | 2136 | 8 | 0 | 0 | 8 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0015 | 0/0 | 2136 | 5 | 4 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0016 | 0/0 | 2136 | 5 | 0 | 0 | 5 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0023 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0024 | 0/0 | 2136 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0046 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0047 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0048 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0056 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0005c0005 | 0/0 | 2136 | 33 | 0 | 0 | 32 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0005c0025 | 0/0 | 2136 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0009 | 0/0 | 2136 | 12 | 0 | 0 | 12 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0013 | 0/0 | 2136 | 5 | 0 | 3 | 1 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0022 | 0/0 | 2136 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0029 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0031 | 0/0 | 2136 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0033 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0055 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0007c0008 | 0/0 | 2136 | 17 | 16 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0008c0018 | 0/0 | 2136 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0009c0017 | 0/0 | 2136 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0010c0052 | 0/0 | 2133 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0010c0053 | 1/0 | 2133 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0011c0035 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0012c0037 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0013c0040 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0014c0039 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0015c0043 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0016c0044 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0017c0045 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0018c0049 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0019c0050 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0020c0051 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0021c0027 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0022c0032 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0023c0028 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0024c0026 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2724 | 75 | 14 | 9 | 39 | 6 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0002t0001 | 0/0 | 2724 | 37 | 9 | 12 | 8 | 0 | 8 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0002t0003 | 0/0 | 2724 | 20 | 0 | 0 | 19 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0007t0001 | 0/0 | 2724 | 13 | 11 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0007t0003 | 0/0 | 2724 | 5 | 5 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0007t0005 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0011t0001 | 0/0 | 2724 | 9 | 1 | 5 | 2 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0014t0001 | 0/0 | 2724 | 5 | 3 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0019t0001 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0019t0003 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0020t0001 | 0/0 | 2724 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0021t0001 | 0/0 | 2724 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0030t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0034t0001 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0001c0054t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0003t0001 | 0/0 | 2724 | 49 | 0 | 4 | 42 | 0 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0006t0001 | 0/1 | 2724 | 23 | 1 | 16 | 0 | 2 | 3 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0036t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0002c0042t0001 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0004t0001 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0004t0002 | 0/0 | 2724 | 42 | 2 | 10 | 17 | 6 | 7 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0038t0002 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0003c0041t0002 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0010t0001 | 0/0 | 2724 | 11 | 0 | 5 | 0 | 0 | 6 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0010t0006 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0012t0001 | 0/0 | 2724 | 8 | 0 | 0 | 8 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0015t0001 | 0/0 | 2724 | 5 | 4 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0016t0001 | 0/0 | 2724 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0016t0003 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0023t0001 | 0/0 | 2724 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0024t0001 | 0/0 | 2724 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0046t0001 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0047t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0048t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0004c0056t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0005c0005t0002 | 0/0 | 2724 | 33 | 0 | 0 | 32 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0005c0025t0002 | 0/0 | 2724 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0009t0002 | 0/0 | 2724 | 12 | 0 | 0 | 12 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0013t0002 | 0/0 | 2724 | 5 | 0 | 3 | 1 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0022t0002 | 0/0 | 2724 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0029t0002 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0031t0002 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0033t0002 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0006c0055t0004 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0007c0008t0001 | 0/0 | 2724 | 17 | 16 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0008c0018t0001 | 0/0 | 2724 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0009c0017t0001 | 0/0 | 2724 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0010c0052t0001 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0010c0053t0001 | 1/0 | 2721 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0011c0035t0002 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0012c0037t0002 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0013c0040t0001 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0014c0039t0001 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0015c0043t0001 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0016c0044t0002 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0017c0045t0002 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0018c0049t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0019c0050t0007 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0020c0051t0001 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0021c0027t0003 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0022c0032t0003 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0023c0028t0001 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
a0024c0026t0003 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | copy fasta | chr3 | 46430645 | 46469905 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0006 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0003g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0007t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0011t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0011t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0011t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0011t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0011t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0014t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0014t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0014t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0019t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0019t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0020t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0020t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0021t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0021t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0030t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0034t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0001c0054t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0004 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0038 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0036t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0002c0042t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0004t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0038t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0003c0041t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0060 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0010t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0012t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0012t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0012t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0012t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0012t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0015t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0015t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0015t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0015t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0016t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0016t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0016t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0016t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0016t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0023t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0024t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0024t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0046t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0047t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0048t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0004c0056t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0025t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0005c0025t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0009t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0013t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0013t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0013t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0013t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0022t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0022t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0029t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0031t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0033t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0006c0055t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0007c0008t0001g0003 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0007c0008t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0007c0008t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0007c0008t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0007c0008t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0007c0008t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0008c0018t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0008c0018t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0008c0018t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0009c0017t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0009c0017t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0010c0052t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0010c0053t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0011c0035t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0012c0037t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0013c0040t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0014c0039t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0015c0043t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0016c0044t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0017c0045t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0018c0049t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0019c0050t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0020c0051t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0021c0027t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0022c0032t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0023c0028t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
a0024c0026t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0006 | c0013 | t0002 | g0216 | EUR | GBR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00099 | hp2 | a0003 | c0004 | t0002 | g0086 | EUR | GBR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | GBR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00140 | hp2 | a0002 | c0006 | t0001 | g0004 | EUR | GBR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00280 | hp1 | a0002 | c0006 | t0001 | g0091 | EUR | FIN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00280 | hp2 | a0003 | c0004 | t0002 | g0146 | EUR | FIN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00423 | hp1 | a0006 | c0009 | t0002 | g0016 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00423 | hp2 | a0006 | c0022 | t0002 | g0209 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00438 | hp2 | a0004 | c0016 | t0001 | g0155 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00544 | hp2 | a0005 | c0005 | t0002 | g0150 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00558 | hp1 | a0006 | c0009 | t0002 | g0029 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00558 | hp2 | a0003 | c0004 | t0001 | g0123 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00597 | hp2 | a0005 | c0005 | t0002 | g0005 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00609 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00639 | hp2 | a0004 | c0010 | t0001 | g0276 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00642 | hp1 | a0003 | c0004 | t0002 | g0112 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00673 | hp1 | a0002 | c0003 | t0001 | g0121 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00738 | hp1 | a0003 | c0004 | t0002 | g0169 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00738 | hp2 | a0002 | c0003 | t0001 | g0126 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00741 | hp1 | a0002 | c0006 | t0001 | g0004 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG00741 | hp2 | a0002 | c0006 | t0001 | g0162 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01069 | hp1 | a0006 | c0031 | t0002 | g0225 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01070 | hp1 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01070 | hp2 | a0003 | c0004 | t0002 | g0031 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01071 | hp1 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01074 | hp1 | a0004 | c0015 | t0001 | g0041 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01074 | hp2 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01081 | hp1 | a0002 | c0006 | t0001 | g0004 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01081 | hp2 | a0003 | c0004 | t0002 | g0093 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01106 | hp1 | a0001 | c0011 | t0001 | g0186 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01109 | hp1 | a0003 | c0004 | t0002 | g0104 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01109 | hp2 | a0007 | c0008 | t0001 | g0003 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01167 | hp1 | a0001 | c0007 | t0001 | g0052 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01167 | hp2 | a0003 | c0004 | t0002 | g0163 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01168 | hp2 | a0004 | c0010 | t0001 | g0060 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01169 | hp1 | a0001 | c0007 | t0001 | g0052 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01169 | hp2 | a0004 | c0010 | t0001 | g0275 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01175 | hp1 | a0002 | c0006 | t0001 | g0004 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01175 | hp2 | a0003 | c0004 | t0002 | g0031 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01192 | hp1 | a0002 | c0006 | t0001 | g0004 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01192 | hp2 | a0001 | c0011 | t0001 | g0184 | AMR | PUR | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01256 | hp1 | a0002 | c0006 | t0001 | g0037 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01256 | hp2 | a0001 | c0011 | t0001 | g0013 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01257 | hp1 | a0002 | c0006 | t0001 | g0004 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01258 | hp2 | a0001 | c0011 | t0001 | g0013 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01261 | hp1 | a0001 | c0011 | t0001 | g0013 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01261 | hp2 | a0002 | c0006 | t0001 | g0168 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01361 | hp1 | a0002 | c0006 | t0001 | g0166 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01361 | hp2 | a0003 | c0004 | t0002 | g0113 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01433 | hp1 | a0001 | c0019 | t0001 | g0284 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01433 | hp2 | a0003 | c0004 | t0002 | g0125 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01496 | hp2 | a0006 | c0013 | t0002 | g0051 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01515 | hp1 | a0003 | c0004 | t0002 | g0116 | EUR | IBS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01516 | hp1 | a0003 | c0004 | t0002 | g0087 | EUR | IBS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01884 | hp1 | a0024 | c0026 | t0003 | g0222 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01891 | hp1 | a0016 | c0044 | t0002 | g0175 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01891 | hp2 | a0007 | c0008 | t0001 | g0009 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01934 | hp1 | a0001 | c0014 | t0001 | g0206 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01952 | hp2 | a0002 | c0006 | t0001 | g0167 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01975 | hp1 | a0006 | c0013 | t0002 | g0051 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01978 | hp1 | a0004 | c0010 | t0001 | g0278 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0021 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01981 | hp1 | a0004 | c0010 | t0001 | g0277 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01993 | hp2 | a0002 | c0003 | t0001 | g0021 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02004 | hp1 | a0002 | c0006 | t0001 | g0038 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02004 | hp2 | a0003 | c0004 | t0002 | g0131 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02015 | hp1 | a0006 | c0009 | t0002 | g0029 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02027 | hp1 | a0006 | c0009 | t0002 | g0245 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02027 | hp2 | a0011 | c0035 | t0002 | g0085 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0204 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02055 | hp1 | a0010 | c0052 | t0001 | g0159 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02055 | hp2 | a0001 | c0007 | t0001 | g0053 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02056 | hp1 | a0003 | c0004 | t0002 | g0124 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02071 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02074 | hp1 | a0005 | c0005 | t0002 | g0005 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0205 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02080 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02083 | hp1 | a0003 | c0004 | t0002 | g0137 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02083 | hp2 | a0006 | c0033 | t0002 | g0260 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02129 | hp2 | a0004 | c0016 | t0001 | g0157 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0047 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02132 | hp2 | a0006 | c0009 | t0002 | g0016 | EAS | KHV | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02145 | hp1 | a0001 | c0011 | t0001 | g0185 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02148 | hp1 | a0006 | c0013 | t0002 | g0211 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02148 | hp2 | a0002 | c0006 | t0001 | g0136 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02165 | hp2 | a0005 | c0005 | t0002 | g0148 | EAS | CDX | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02257 | hp1 | a0004 | c0024 | t0001 | g0180 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02257 | hp2 | a0002 | c0006 | t0001 | g0170 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02258 | hp2 | a0008 | c0018 | t0001 | g0069 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02280 | hp1 | a0001 | c0014 | t0001 | g0023 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02293 | hp2 | a0002 | c0003 | t0001 | g0108 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02300 | hp1 | a0001 | c0014 | t0001 | g0023 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02300 | hp2 | a0002 | c0006 | t0001 | g0004 | AMR | PEL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02451 | hp1 | a0007 | c0008 | t0001 | g0009 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02572 | hp2 | a0001 | c0007 | t0001 | g0220 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02615 | hp1 | a0002 | c0036 | t0001 | g0096 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02615 | hp2 | a0004 | c0015 | t0001 | g0178 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02622 | hp1 | a0007 | c0008 | t0001 | g0003 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02622 | hp2 | a0007 | c0008 | t0001 | g0009 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02630 | hp1 | a0017 | c0045 | t0002 | g0176 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02630 | hp2 | a0007 | c0008 | t0001 | g0003 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02647 | hp1 | a0018 | c0049 | t0001 | g0073 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02683 | hp1 | a0002 | c0006 | t0001 | g0165 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02683 | hp2 | a0004 | c0010 | t0001 | g0279 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02698 | hp2 | a0003 | c0041 | t0002 | g0161 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02717 | hp1 | a0001 | c0007 | t0003 | g0026 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02717 | hp2 | a0001 | c0021 | t0001 | g0230 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02723 | hp1 | a0007 | c0008 | t0001 | g0003 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0285 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02738 | hp2 | a0003 | c0004 | t0002 | g0122 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02809 | hp1 | a0007 | c0008 | t0001 | g0079 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02809 | hp2 | a0001 | c0007 | t0001 | g0224 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02818 | hp1 | a0004 | c0015 | t0001 | g0177 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02818 | hp2 | a0004 | c0024 | t0001 | g0062 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02896 | hp1 | a0007 | c0008 | t0001 | g0003 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02896 | hp2 | a0004 | c0023 | t0001 | g0040 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02897 | hp1 | a0007 | c0008 | t0001 | g0003 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02897 | hp2 | a0004 | c0023 | t0001 | g0040 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02922 | hp1 | a0001 | c0014 | t0001 | g0023 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02922 | hp2 | a0001 | c0007 | t0001 | g0025 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02965 | hp1 | a0019 | c0050 | t0007 | g0075 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02965 | hp2 | a0004 | c0015 | t0001 | g0179 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02970 | hp1 | a0004 | c0048 | t0001 | g0287 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02976 | hp1 | a0001 | c0054 | t0001 | g0078 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02976 | hp2 | a0007 | c0008 | t0001 | g0082 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03017 | hp1 | a0003 | c0004 | t0002 | g0119 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03041 | hp1 | a0007 | c0008 | t0001 | g0080 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03041 | hp2 | a0001 | c0007 | t0005 | g0226 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03130 | hp1 | a0001 | c0007 | t0001 | g0227 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03130 | hp2 | a0001 | c0030 | t0001 | g0171 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03139 | hp1 | a0001 | c0007 | t0003 | g0228 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03139 | hp2 | a0006 | c0055 | t0004 | g0063 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03195 | hp1 | a0004 | c0015 | t0001 | g0041 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03195 | hp2 | a0001 | c0007 | t0003 | g0026 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03209 | hp1 | a0004 | c0047 | t0001 | g0061 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03209 | hp2 | a0007 | c0008 | t0001 | g0009 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03225 | hp1 | a0001 | c0020 | t0001 | g0268 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03225 | hp2 | a0007 | c0008 | t0001 | g0003 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03453 | hp1 | a0001 | c0007 | t0001 | g0025 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03453 | hp2 | a0008 | c0018 | t0001 | g0068 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03486 | hp1 | a0007 | c0008 | t0001 | g0003 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03490 | hp2 | a0004 | c0010 | t0001 | g0060 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03491 | hp1 | a0002 | c0006 | t0001 | g0130 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03491 | hp2 | a0004 | c0010 | t0001 | g0273 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03516 | hp1 | a0001 | c0020 | t0001 | g0267 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03516 | hp2 | a0001 | c0007 | t0001 | g0053 | AFR | ESN | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03540 | hp1 | a0021 | c0027 | t0003 | g0232 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03540 | hp2 | a0003 | c0004 | t0002 | g0094 | AFR | GWD | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03579 | hp2 | a0001 | c0007 | t0003 | g0026 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0196 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03669 | hp2 | a0004 | c0010 | t0001 | g0270 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03688 | hp1 | a0003 | c0004 | t0002 | g0033 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03704 | hp1 | a0004 | c0010 | t0006 | g0274 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03704 | hp2 | a0006 | c0029 | t0002 | g0065 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03710 | hp1 | a0004 | c0010 | t0001 | g0269 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03834 | hp2 | a0001 | c0011 | t0001 | g0013 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03927 | hp1 | a0002 | c0006 | t0001 | g0037 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03942 | hp1 | a0023 | c0028 | t0001 | g0240 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0133 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04115 | hp1 | a0003 | c0004 | t0002 | g0109 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0215 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04184 | hp1 | a0012 | c0037 | t0002 | g0103 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0083 | SAS | BEB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04199 | hp1 | a0003 | c0004 | t0002 | g0033 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04199 | hp2 | a0005 | c0005 | t0002 | g0005 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04204 | hp1 | a0003 | c0004 | t0002 | g0145 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04204 | hp2 | a0004 | c0010 | t0001 | g0071 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04228 | hp1 | a0003 | c0004 | t0002 | g0134 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18522 | hp1 | a0001 | c0007 | t0001 | g0054 | AFR | YRI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18522 | hp2 | a0001 | c0014 | t0001 | g0173 | AFR | YRI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18612 | hp1 | a0004 | c0012 | t0001 | g0072 | EAS | CHB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18747 | hp1 | a0015 | c0043 | t0001 | g0139 | EAS | CHB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0214 | EAS | CHB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | YRI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18940 | hp1 | a0006 | c0013 | t0002 | g0217 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18940 | hp2 | a0002 | c0003 | t0001 | g0140 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0105 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18942 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18945 | hp1 | a0005 | c0025 | t0002 | g0281 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18945 | hp2 | a0004 | c0046 | t0001 | g0149 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18946 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18947 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18948 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18948 | hp2 | a0003 | c0004 | t0002 | g0142 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18951 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18951 | hp2 | a0005 | c0005 | t0002 | g0039 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18954 | hp1 | a0004 | c0012 | t0001 | g0017 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18954 | hp2 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18957 | hp2 | a0005 | c0005 | t0002 | g0005 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18959 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18959 | hp2 | a0005 | c0005 | t0002 | g0005 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18960 | hp2 | a0001 | c0011 | t0001 | g0042 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18961 | hp1 | a0009 | c0017 | t0001 | g0055 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18962 | hp2 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18963 | hp1 | a0003 | c0004 | t0002 | g0118 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18964 | hp1 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18964 | hp2 | a0003 | c0004 | t0002 | g0036 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18965 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18965 | hp2 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18966 | hp2 | a0004 | c0016 | t0001 | g0264 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18967 | hp2 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18968 | hp2 | a0006 | c0009 | t0002 | g0234 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18970 | hp1 | a0004 | c0012 | t0001 | g0282 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18970 | hp2 | a0004 | c0016 | t0001 | g0158 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18972 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18974 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18974 | hp2 | a0006 | c0009 | t0002 | g0247 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18975 | hp1 | a0003 | c0004 | t0002 | g0095 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18975 | hp2 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18978 | hp1 | a0002 | c0003 | t0001 | g0097 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18978 | hp2 | a0001 | c0034 | t0001 | g0262 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18979 | hp2 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18980 | hp1 | a0002 | c0042 | t0001 | g0138 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18982 | hp1 | a0003 | c0004 | t0002 | g0036 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18982 | hp2 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18983 | hp1 | a0003 | c0038 | t0002 | g0066 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18983 | hp2 | a0005 | c0005 | t0002 | g0156 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18984 | hp2 | a0004 | c0012 | t0001 | g0017 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18986 | hp1 | a0022 | c0032 | t0003 | g0181 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18987 | hp2 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0098 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18989 | hp1 | a0006 | c0009 | t0002 | g0252 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18989 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18990 | hp2 | a0006 | c0009 | t0002 | g0248 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18991 | hp2 | a0006 | c0022 | t0002 | g0207 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18992 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18992 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18993 | hp1 | a0005 | c0025 | t0002 | g0280 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18993 | hp2 | a0006 | c0009 | t0002 | g0016 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18997 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18997 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19000 | hp1 | a0005 | c0005 | t0002 | g0147 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0106 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19001 | hp2 | a0005 | c0005 | t0002 | g0164 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19002 | hp2 | a0005 | c0005 | t0002 | g0005 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19003 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19004 | hp2 | a0005 | c0005 | t0002 | g0005 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19005 | hp2 | a0006 | c0009 | t0002 | g0016 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19006 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19006 | hp2 | a0005 | c0005 | t0002 | g0152 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19007 | hp1 | a0005 | c0005 | t0002 | g0154 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19009 | hp2 | a0005 | c0005 | t0002 | g0151 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19011 | hp1 | a0001 | c0011 | t0001 | g0042 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19012 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19030 | hp1 | a0008 | c0018 | t0001 | g0286 | AFR | LWK | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19030 | hp2 | a0001 | c0007 | t0003 | g0223 | AFR | LWK | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | LWK | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19056 | hp1 | a0005 | c0005 | t0002 | g0039 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19058 | hp1 | a0003 | c0004 | t0002 | g0115 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19060 | hp1 | a0004 | c0012 | t0001 | g0271 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19062 | hp1 | a0003 | c0004 | t0002 | g0135 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19064 | hp2 | a0009 | c0017 | t0001 | g0055 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19066 | hp1 | a0003 | c0004 | t0002 | g0127 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19066 | hp2 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19067 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19068 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19072 | hp1 | a0003 | c0004 | t0002 | g0107 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19074 | hp1 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19076 | hp1 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19076 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19077 | hp1 | a0002 | c0003 | t0001 | g0102 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19079 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19080 | hp2 | a0004 | c0012 | t0001 | g0272 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19081 | hp1 | a0003 | c0004 | t0002 | g0141 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19081 | hp2 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19083 | hp1 | a0005 | c0005 | t0002 | g0001 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19084 | hp1 | a0014 | c0039 | t0001 | g0120 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19084 | hp2 | a0004 | c0012 | t0001 | g0017 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19085 | hp2 | a0009 | c0017 | t0001 | g0261 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19086 | hp1 | a0003 | c0004 | t0002 | g0128 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19090 | hp1 | a0004 | c0016 | t0003 | g0153 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19090 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19091 | hp2 | a0006 | c0009 | t0002 | g0249 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | YRI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA19240 | hp2 | a0007 | c0008 | t0001 | g0081 | AFR | YRI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20129 | hp2 | a0001 | c0021 | t0001 | g0221 | AFR | ASW | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20752 | hp1 | a0003 | c0004 | t0002 | g0129 | EUR | TSI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20752 | hp2 | a0013 | c0040 | t0001 | g0132 | EUR | TSI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20805 | hp2 | a0003 | c0004 | t0002 | g0114 | EUR | TSI | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02109 | hp1 | a0001 | c0007 | t0001 | g0025 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02109 | hp2 | a0003 | c0004 | t0002 | g0092 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02486 | hp1 | a0020 | c0051 | t0001 | g0074 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | USA | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
HG06807 | hp2 | a0007 | c0008 | t0001 | g0003 | AFR | USA | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA18955 | hp2 | a0004 | c0012 | t0001 | g0017 | EAS | JPT | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20300 | hp1 | a0001 | c0007 | t0001 | g0054 | AFR | USA | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA20300 | hp2 | a0004 | c0056 | t0001 | g0077 | AFR | USA | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA21309 | hp1 | a0001 | c0007 | t0001 | g0231 | AFR | LWK | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
NA21309 | hp2 | a0001 | c0019 | t0003 | g0229 | AFR | LWK | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
homoSapiens_chm13v2 | hp1 | a0002 | c0006 | t0001 | g0038 | REF | REF | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
homoSapiens_grch38 | hp1 | a0010 | c0053 | t0001 | g0160 | REF | REF | LTF_chr3_46430645_46469905 | LTF | chr3 | 46430645 | 46469905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46439363
|
G | A | 1 | a0013 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1841C>T | p.Pro614Leu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1879/2721 | 1841/2133 | 614/710 | chr3 | 46439363 | ||
chr3:46439364
|
G | A | 1 | a0017 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1840C>T | p.Pro614Ser | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1878/2721 | 1840/2133 | 614/710 | chr3 | 46439364 | ||
chr3:46439418
|
C | T | 1 | a0014 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1786G>A | p.Asp596Asn | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1824/2721 | 1786/2133 | 596/710 | chr3 | 46439418 | ||
chr3:46439467
|
C | A | 1 | a0003 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1737G>T | p.Glu579Asp | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1775/2721 | 1737/2133 | 579/710 | chr3 | 46439467 | ||
chr3:46439467
|
C | G | 8 | a0003a0005a0006others(5): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
missense_variant | MODERATE | c.1737G>C | p.Glu579Asp | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1775/2721 | 1737/2133 | 579/710 | chr3 | 46439467 | ||
chr3:46443487
|
C | T | 1 | a0018 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1609G>A | p.Val537Met | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/17 | 1647/2721 | 1609/2133 | 537/710 | chr3 | 46443487 | ||
chr3:46446446
|
C | G | 1 | a0012 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1351G>C | p.Val451Leu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/17 | 1389/2721 | 1351/2133 | 451/710 | chr3 | 46446446 | ||
chr3:46448922
|
C | T | 1 | a0022 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.1153G>A | p.Glu385Lys | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/17 | 1191/2721 | 1153/2133 | 385/710 | chr3 | 46448922 | ||
chr3:46449006
|
C | A | 2 | a0016a0017 | 2 | HG01891.hp1 HG02630.hp1 |
missense_variant | MODERATE | c.1069G>T | p.Val357Leu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/17 | 1107/2721 | 1069/2133 | 357/710 | chr3 | 46449006 | ||
chr3:46450019
|
C | T | 1 | a0023 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.892G>A | p.Gly298Arg | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/17 | 930/2721 | 892/2133 | 298/710 | chr3 | 46450019 | ||
chr3:46450575
|
G | A | 1 | a0015 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.802C>T | p.Arg268Trp | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/17 | 840/2721 | 802/2133 | 268/710 | chr3 | 46450575 | ||
chr3:46450659
|
C | T | 1 | a0009 | 3 | NA18961.hp1 NA19064.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.718G>A | p.Glu240Lys | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/17 | 756/2721 | 718/2133 | 240/710 | chr3 | 46450659 | ||
chr3:46455364
|
G | A | 4 | a0007a0018a0019others(1): Show | 20 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(17): Show |
missense_variant | MODERATE | c.578C>T | p.Ala193Val | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/17 | 616/2721 | 578/2133 | 193/710 | chr3 | 46455364 | ||
chr3:46455373
|
C | T | 1 | a0021 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.569G>A | p.Arg190His | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/17 | 607/2721 | 569/2133 | 190/710 | chr3 | 46455373 | ||
chr3:46455852
|
A | G | 1 | a0024 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.443T>C | p.Ile148Thr | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 4/17 | 481/2721 | 443/2133 | 148/710 | chr3 | 46455852 | ||
chr3:46459678
|
A | T | 1 | a0008 | 3 | HG02258.hp2 HG03453.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.185T>A | p.Ile62Asn | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/17 | 223/2721 | 185/2133 | 62/710 | chr3 | 46459678 | ||
chr3:46459723
|
T | C | 16 | a0001a0004a0005others(13): Show | 302 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(299): Show |
missense_variant | MODERATE | c.140A>G | p.Lys47Arg | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/17 | 178/2721 | 140/2133 | 47/710 | chr3 | 46459723 | ||
chr3:46459775
|
C | G | 1 | a0011 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.88G>C | p.Val30Leu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/17 | 126/2721 | 88/2133 | 30/710 | chr3 | 46459775 | ||
chr3:46459778
|
C | T | 8 | a0001a0006a0007others(5): Show | 221 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(218): Show |
missense_variant | MODERATE | c.85G>A | p.Ala29Thr | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/17 | 123/2721 | 85/2133 | 29/710 | chr3 | 46459778 | ||
chr3:46459794
|
C | CCTT | 23 | a0001a0002a0003others(20): Show | 426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
disruptive_inframe_insertion | MODERATE | c.68_69insAAG | p.Arg23dup | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/17 | 106/2721 | 68/2133 | 23/710 | chr3 | 46459794 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46437977
|
G | A | 1 | a0004c0047 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2061C>T | p.Val687Val | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/17 | 2099/2721 | 2061/2133 | 687/710 | chr3 | 46437977 | ||
chr3:46439310
|
A | G | 24 | a0001c0001a0001c0002a0001c0007others(21): Show | 270 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(267): Show |
synonymous_variant | LOW | c.1894T>C | p.Leu632Leu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1932/2721 | 1894/2133 | 632/710 | chr3 | 46439310 | ||
chr3:46439326
|
T | C | 1 | a0010c0052 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1878A>G | p.Glu626Glu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/17 | 1916/2721 | 1878/2133 | 626/710 | chr3 | 46439326 | ||
chr3:46443473
|
G | A | 24 | a0001c0001a0001c0002a0001c0011others(21): Show | 240 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
synonymous_variant | LOW | c.1623C>T | p.Asn541Asn | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/17 | 1661/2721 | 1623/2133 | 541/710 | chr3 | 46443473 | ||
chr3:46447363
|
T | C | 9 | a0001c0002a0001c0014a0001c0030others(6): Show | 89 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(86): Show |
synonymous_variant | LOW | c.1248A>G | p.Gly416Gly | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 10/17 | 1286/2721 | 1248/2133 | 416/710 | chr3 | 46447363 | ||
chr3:46448875
|
G | A | 9 | a0001c0002a0001c0011a0001c0014others(6): Show | 90 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(87): Show |
synonymous_variant | LOW | c.1200C>T | p.Ile400Ile | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/17 | 1238/2721 | 1200/2133 | 400/710 | chr3 | 46448875 | ||
chr3:46448965
|
G | A | 4 | a0001c0007a0001c0021a0006c0031others(1): Show | 23 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
synonymous_variant | LOW | c.1110C>T | p.Gly370Gly | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/17 | 1148/2721 | 1110/2133 | 370/710 | chr3 | 46448965 | ||
chr3:46448983
|
G | A | 10 | a0001c0002a0001c0011a0001c0014others(7): Show | 102 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(99): Show |
synonymous_variant | LOW | c.1092C>T | p.Val364Val | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/17 | 1130/2721 | 1092/2133 | 364/710 | chr3 | 46448983 | ||
chr3:46450495
|
C | T | 1 | a0002c0036 | 1 | HG02615.hp1 | splice_region_variant&synonymous_variant | LOW | c.882G>A | p.Gln294Gln | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/17 | 920/2721 | 882/2133 | 294/710 | chr3 | 46450495 | ||
chr3:46454336
|
G | A | 1 | a0006c0033 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.672C>T | p.Asp224Asp | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/17 | 710/2721 | 672/2133 | 224/710 | chr3 | 46454336 | ||
chr3:46455321
|
C | T | 1 | a0010c0052 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.621G>A | p.Pro207Pro | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/17 | 659/2721 | 621/2133 | 207/710 | chr3 | 46455321 | ||
chr3:46455408
|
G | A | 1 | a0006c0055 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.534C>T | p.Pro178Pro | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/17 | 572/2721 | 534/2133 | 178/710 | chr3 | 46455408 | ||
chr3:46455878
|
G | T | 3 | a0004c0023a0016c0044a0017c0045 | 4 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.417C>A | p.Arg139Arg | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 4/17 | 455/2721 | 417/2133 | 139/710 | chr3 | 46455878 | ||
chr3:46455914
|
T | C | 1 | a0001c0034 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.381A>G | p.Glu127Glu | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 4/17 | 419/2721 | 381/2133 | 127/710 | chr3 | 46455914 | ||
chr3:46459818
|
T | C | 4 | a0001c0054a0004c0056a0006c0055others(1): Show | 20 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(17): Show |
splice_region_variant&synonymous_variant | LOW | c.45A>G | p.Gly15Gly | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/17 | 83/2721 | 45/2133 | 15/710 | chr3 | 46459818 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46435652
|
C | G | 1 | a0006c0055t0004 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 17/17 | 543 | chr3 | 46435652 | |||||
chr3:46435658
|
C | T | 1 | a0001c0007t0005 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 17/17 | 537 | chr3 | 46435658 | |||||
chr3:46435731
|
C | T | 17 | a0003c0004t0002a0003c0038t0002a0003c0041t0002others(14): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*464G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 17/17 | 464 | chr3 | 46435731 | |||||
chr3:46435785
|
G | A | 1 | a0004c0010t0006 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 17/17 | 410 | chr3 | 46435785 | |||||
chr3:46435811
|
C | A | 7 | a0001c0002t0003a0001c0007t0003a0001c0019t0003others(4): Show | 30 | HG01884.hp1 HG02040.hp1 HG02071.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*384G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 17/17 | 384 | chr3 | 46435811 | |||||
chr3:46436067
|
G | C | 1 | a0019c0050t0007 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 17/17 | 128 | chr3 | 46436067 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46436247
|
G | A | 1 | a0001c0030t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2099-18C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436247 | ||||||
chr3:46436335
|
C | T | 36 | a0001c0002t0003g0044a0001c0002t0003g0046a0001c0002t0003g0047others(33): Show | 51 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2099-106G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436335 | ||||||
chr3:46436339
|
C | T | 36 | a0001c0002t0003g0044a0001c0002t0003g0046a0001c0002t0003g0047others(33): Show | 51 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2099-110G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436339 | ||||||
chr3:46436408
|
G | A | 1 | a0002c0006t0001g0167 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2099-179C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436408 | ||||||
chr3:46436437
|
G | C | 2 | a0002c0003t0001g0108a0004c0010t0001g0278 | 2 | HG01978.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2099-208C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436437 | ||||||
chr3:46436526
|
T | C | 1 | a0001c0002t0001g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2099-297A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436526 | ||||||
chr3:46436549
|
G | A | 1 | a0008c0018t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2099-320C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436549 | ||||||
chr3:46436645
|
A | C | 5 | a0002c0003t0001g0010a0002c0003t0001g0097a0002c0003t0001g0099others(2): Show | 8 | NA18961.hp2 NA18963.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.2099-416T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436645 | ||||||
chr3:46436713
|
G | A | 7 | a0001c0014t0001g0206a0001c0030t0001g0171a0004c0024t0001g0062others(4): Show | 7 | HG01934.hp1 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2099-484C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436713 | ||||||
chr3:46436826
|
C | T | 1 | a0004c0047t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2099-597G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436826 | ||||||
chr3:46436899
|
C | G | 1 | a0001c0030t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2099-670G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436899 | ||||||
chr3:46436965
|
C | T | 2 | a0001c0007t0001g0054a0001c0007t0001g0224 | 3 | HG02809.hp2 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2099-736G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46436965 | ||||||
chr3:46437004
|
T | C | 1 | a0007c0008t0001g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2099-775A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437004 | ||||||
chr3:46437072
|
C | A | 1 | a0008c0018t0001g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2099-843G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437072 | ||||||
chr3:46437320
|
A | AT | 139 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(136): Show | 204 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(201): Show |
intron_variant | MODIFIER | c.2098+619dupA | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437320 | ||||||
chr3:46437320
|
A | ATT | 101 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0058others(98): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2098+618_2098+619d others(4): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437320 | ||||||
chr3:46437321
|
T | TC | 9 | a0001c0001t0001g0027a0001c0001t0001g0067a0004c0023t0001g0040others(6): Show | 23 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2098+618_2098+619i others(3): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437321 | ||||||
chr3:46437375
|
C | T | 63 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0002t0001g0050others(60): Show | 97 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.2098+565G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437375 | ||||||
chr3:46437437
|
C | A | 1 | a0007c0008t0001g0081 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2098+503G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437437 | ||||||
chr3:46437445
|
CA | C | 63 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0002t0001g0050others(60): Show | 97 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.2098+494delT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437445 | ||||||
chr3:46437515
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2098+425C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437515 | ||||||
chr3:46437577
|
C | T | 5 | a0001c0020t0001g0267a0001c0020t0001g0268a0001c0054t0001g0078others(2): Show | 5 | HG02647.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2098+363G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437577 | ||||||
chr3:46437588
|
G | A | 2 | a0003c0004t0002g0128a0020c0051t0001g0074 | 2 | HG02486.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2098+352C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437588 | ||||||
chr3:46437617
|
G | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(271): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.2098+323C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437617 | ||||||
chr3:46437717
|
A | G | 205 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0219others(202): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2098+223T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437717 | ||||||
chr3:46437727
|
G | A | 1 | a0002c0006t0001g0162 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2098+213C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437727 | ||||||
chr3:46437762
|
C | A | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2098+178G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437762 | ||||||
chr3:46437818
|
A | G | 1 | a0004c0047t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2098+122T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437818 | ||||||
chr3:46437858
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2098+82C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437858 | ||||||
chr3:46437914
|
G | A | 1 | a0004c0047t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2098+26C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 16/16 | chr3 | 46437914 | ||||||
chr3:46438177
|
A | G | 144 | a0001c0001t0001g0219a0001c0001t0001g0239a0001c0001t0001g0254others(141): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1909-48T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438177 | ||||||
chr3:46438249
|
G | C | 2 | a0004c0010t0001g0269a0004c0010t0001g0277 | 2 | HG01981.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1909-120C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438249 | ||||||
chr3:46438339
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1909-210C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438339 | ||||||
chr3:46438394
|
T | G | 1 | a0002c0003t0001g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1909-265A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438394 | ||||||
chr3:46438396
|
T | G | 1 | a0002c0003t0001g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1909-267A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438396 | ||||||
chr3:46438515
|
G | A | 2 | a0001c0002t0003g0190a0001c0002t0003g0204 | 2 | HG02040.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1909-386C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438515 | ||||||
chr3:46438606
|
G | T | 1 | a0004c0016t0001g0158 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1909-477C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438606 | ||||||
chr3:46438618
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1909-489C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438618 | ||||||
chr3:46438681
|
A | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1909-552T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438681 | ||||||
chr3:46438728
|
C | G | 1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1908+568G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438728 | ||||||
chr3:46438859
|
T | C | 1 | a0019c0050t0007g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1908+437A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438859 | ||||||
chr3:46438896
|
C | T | 73 | a0003c0004t0001g0123a0003c0004t0002g0011a0003c0004t0002g0031others(70): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1908+400G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438896 | ||||||
chr3:46438937
|
C | G | 5 | a0001c0020t0001g0267a0001c0020t0001g0268a0001c0054t0001g0078others(2): Show | 5 | HG02647.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1908+359G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46438937 | ||||||
chr3:46439031
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1908+265G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46439031 | ||||||
chr3:46439147
|
C | T | 1 | a0004c0047t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1908+149G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46439147 | ||||||
chr3:46439211
|
G | C | 64 | a0001c0001t0001g0219a0001c0001t0001g0239a0001c0001t0001g0254others(61): Show | 94 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1908+85C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 15/16 | chr3 | 46439211 | ||||||
chr3:46439503
|
A | G | 28 | a0003c0004t0002g0011a0003c0004t0002g0031a0003c0004t0002g0033others(25): Show | 33 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1724-23T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439503 | ||||||
chr3:46439644
|
C | T | 2 | a0003c0004t0002g0031a0003c0004t0002g0114 | 3 | HG01070.hp2 HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1724-164G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439644 | ||||||
chr3:46439670
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 98 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1724-190C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439670 | ||||||
chr3:46439805
|
G | A | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1724-325C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439805 | ||||||
chr3:46439808
|
G | A | 4 | a0003c0004t0002g0131a0006c0013t0002g0051a0006c0013t0002g0211others(1): Show | 5 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-328C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439808 | ||||||
chr3:46439809
|
G | A | 4 | a0003c0004t0002g0131a0006c0013t0002g0051a0006c0013t0002g0211others(1): Show | 5 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-329C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439809 | ||||||
chr3:46439810
|
C | T | 4 | a0003c0004t0002g0131a0006c0013t0002g0051a0006c0013t0002g0211others(1): Show | 5 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-330G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439810 | ||||||
chr3:46439811
|
T | C | 4 | a0003c0004t0002g0131a0006c0013t0002g0051a0006c0013t0002g0211others(1): Show | 5 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-331A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439811 | ||||||
chr3:46439813
|
A | C | 4 | a0003c0004t0002g0131a0006c0013t0002g0051a0006c0013t0002g0211others(1): Show | 5 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-333T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439813 | ||||||
chr3:46439814
|
T | A | 4 | a0003c0004t0002g0131a0006c0013t0002g0051a0006c0013t0002g0211others(1): Show | 5 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-334A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439814 | ||||||
chr3:46439814
|
T | C | 17 | a0001c0002t0001g0050a0001c0002t0001g0210a0001c0002t0001g0215others(14): Show | 22 | HG01168.hp2 HG01169.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.1724-334A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439814 | ||||||
chr3:46439853
|
A | G | 1 | a0003c0004t0001g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1724-373T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439853 | ||||||
chr3:46439909
|
CA | C | 74 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0239others(71): Show | 118 | HG00621.hp2 HG00639.hp1 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.1724-430delT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439909 | ||||||
chr3:46439925
|
C | T | 5 | a0001c0020t0001g0267a0001c0020t0001g0268a0001c0054t0001g0078others(2): Show | 5 | HG02647.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-445G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439925 | ||||||
chr3:46439959
|
C | CCAGCCTA others(6): Show |
2 | a0003c0004t0002g0031a0003c0004t0002g0114 | 3 | HG01070.hp2 HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1724-480_1724-479i others(15): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439959 | ||||||
chr3:46439972
|
A | G | 73 | a0003c0004t0001g0123a0003c0004t0002g0011a0003c0004t0002g0031others(70): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1724-492T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46439972 | ||||||
chr3:46440007
|
A | G | 5 | a0001c0002t0003g0046a0001c0002t0003g0194a0001c0002t0003g0203others(2): Show | 6 | NA18966.hp1 NA18975.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1724-527T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46440007 | ||||||
chr3:46440073
|
C | G | 24 | a0001c0002t0003g0044a0001c0002t0003g0046a0001c0002t0003g0047others(21): Show | 30 | HG01884.hp1 HG02040.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1724-593G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46440073 | ||||||
chr3:46440125
|
A | C | 5 | a0001c0020t0001g0267a0001c0020t0001g0268a0001c0054t0001g0078others(2): Show | 5 | HG02647.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1724-645T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46440125 | ||||||
chr3:46440558
|
C | G | 22 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0014t0001g0023others(19): Show | 45 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1723+858G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46440558 | ||||||
chr3:46440728
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0067a0004c0023t0001g0040others(6): Show | 23 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1723+688C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46440728 | ||||||
chr3:46440784
|
G | C | 1 | a0006c0009t0002g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1723+632C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46440784 | ||||||
chr3:46441006
|
T | C | 1 | a0001c0002t0001g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1723+410A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46441006 | ||||||
chr3:46441096
|
G | C | 1 | a0001c0001t0001g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1723+320C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46441096 | ||||||
chr3:46441176
|
A | AGT | 131 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0239others(128): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1723+238_1723+239d others(4): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46441176 | ||||||
chr3:46441192
|
T | A | 23 | a0001c0002t0001g0050a0001c0002t0001g0210a0001c0002t0001g0215others(20): Show | 30 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1723+224A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46441192 | ||||||
chr3:46441192
|
T | TGTGA | 58 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 98 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1723+223_1723+224i others(6): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46441192 | ||||||
chr3:46441370
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1723+46C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 14/16 | chr3 | 46441370 | ||||||
chr3:46441489
|
A | T | 4 | a0002c0006t0001g0004a0002c0006t0001g0091a0002c0006t0001g0136others(1): Show | 10 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1656-6T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441489 | ||||||
chr3:46441509
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0218others(2): Show | 8 | HG00621.hp1 HG00673.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1656-26T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441509 | ||||||
chr3:46441577
|
A | G | 1 | a0001c0030t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1656-94T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441577 | ||||||
chr3:46441860
|
G | A | 12 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0002t0001g0202others(9): Show | 13 | HG01074.hp1 HG02615.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1656-377C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441860 | ||||||
chr3:46441863
|
G | A | 1 | a0008c0018t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1656-380C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441863 | ||||||
chr3:46441899
|
C | CAGAG | 3 | a0002c0006t0001g0165a0002c0006t0001g0167a0002c0006t0001g0170 | 3 | HG01952.hp2 HG02257.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1656-420_1656-417d others(6): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441899 | ||||||
chr3:46441899
|
CAGAG | C | 6 | a0002c0003t0001g0034a0002c0003t0001g0089a0002c0003t0001g0108others(3): Show | 8 | HG00621.hp2 HG01496.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1656-420_1656-417d others(6): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441899 | ||||||
chr3:46441899
|
CAGAGAGA others(3): Show |
C | 1 | a0002c0042t0001g0138 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1656-426_1656-417d others(12): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441899 | ||||||
chr3:46441920
|
AGAGAGAG others(27): Show |
A | 3 | a0001c0001t0001g0056a0001c0001t0001g0246a0001c0001t0001g0259 | 4 | HG00642.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656-471_1656-438d others(36): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441920 | ||||||
chr3:46441922
|
AGAGAGAG others(19): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1656-465_1656-440d others(28): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441922 | ||||||
chr3:46441924
|
AGAGAGAG others(5): Show |
A | 1 | a0002c0003t0001g0111 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1656-453_1656-442d others(14): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441924 | ||||||
chr3:46441924
|
AGAGAGAG others(7): Show |
A | 1 | a0002c0003t0001g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1656-455_1656-442d others(16): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441924 | ||||||
chr3:46441924
|
AGAGAGAG others(9): Show |
A | 1 | a0002c0003t0001g0121 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1656-457_1656-442d others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441924 | ||||||
chr3:46441924
|
AGAGAGAG others(11): Show |
A | 1 | a0006c0009t0002g0247 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1656-459_1656-442d others(20): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441924 | ||||||
chr3:46441924
|
AGAGAGAG others(23): Show |
A | 40 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(37): Show | 81 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1656-471_1656-442d others(32): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441924 | ||||||
chr3:46441926
|
AGAGAGAG others(5): Show |
A | 2 | a0001c0001t0001g0254a0001c0002t0003g0194 | 2 | NA18984.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1656-455_1656-444d others(14): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441926 | ||||||
chr3:46441926
|
AGAGAGAG others(7): Show |
A | 2 | a0001c0002t0001g0201a0001c0002t0001g0202 | 2 | NA18998.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1656-457_1656-444d others(16): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441926 | ||||||
chr3:46441926
|
AGAGAGAG others(9): Show |
A | 1 | a0001c0001t0001g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1656-459_1656-444d others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441926 | ||||||
chr3:46441926
|
AGAGAGAG others(11): Show |
A | 2 | a0001c0019t0003g0229a0008c0018t0001g0286 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1656-461_1656-444d others(20): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441926 | ||||||
chr3:46441926
|
AGAGAGAG others(21): Show |
A | 5 | a0001c0001t0001g0070a0001c0001t0001g0250a0001c0001t0001g0251others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1656-471_1656-444d others(30): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441926 | ||||||
chr3:46441926
|
AGAGAGAG others(23): Show |
A | 2 | a0001c0001t0001g0253a0004c0016t0001g0158 | 2 | HG03654.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1656-473_1656-444d others(32): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441926 | ||||||
chr3:46441928
|
AGAGAGAG others(1): Show |
A | 4 | a0001c0002t0001g0191a0003c0004t0002g0033a0003c0004t0002g0145others(1): Show | 5 | HG01981.hp2 HG02647.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1656-453_1656-446d others(10): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(3): Show |
A | 6 | a0001c0002t0001g0006a0001c0002t0001g0193a0001c0002t0001g0212others(3): Show | 11 | HG00735.hp1 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1656-455_1656-446d others(12): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(5): Show |
A | 3 | a0001c0002t0001g0210a0003c0004t0002g0092a0006c0022t0002g0207 | 3 | HG02109.hp2 HG03239.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1656-457_1656-446d others(14): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(7): Show |
A | 4 | a0001c0002t0001g0022a0001c0002t0001g0182a0001c0002t0001g0188others(1): Show | 6 | HG00639.hp1 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656-459_1656-446d others(16): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(9): Show |
A | 1 | a0001c0011t0001g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1656-461_1656-446d others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(11): Show |
A | 2 | a0001c0007t0001g0220a0002c0006t0001g0136 | 2 | HG02148.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1656-463_1656-446d others(20): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(13): Show |
A | 9 | a0001c0002t0001g0189a0001c0007t0001g0025a0001c0007t0001g0052others(6): Show | 18 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1656-465_1656-446d others(22): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(19): Show |
A | 2 | a0001c0002t0001g0183a0001c0011t0001g0185 | 2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1656-471_1656-446d others(28): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441928
|
AGAGAGAG others(21): Show |
A | 1 | a0001c0011t0001g0186 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1656-473_1656-446d others(30): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441928 | ||||||
chr3:46441930
|
AGAGAGT | A | 16 | a0002c0003t0001g0019a0002c0003t0001g0035a0002c0003t0001g0088others(13): Show | 22 | HG00099.hp1 HG01167.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.1656-453_1656-448d others(8): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(1): Show |
A | 25 | a0001c0001t0001g0027a0001c0001t0001g0067a0002c0003t0001g0010others(22): Show | 36 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1656-455_1656-448d others(10): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(3): Show |
A | 8 | a0001c0001t0001g0257a0001c0002t0001g0200a0002c0003t0001g0021others(5): Show | 10 | HG01978.hp2 HG01993.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1656-457_1656-448d others(12): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(5): Show |
A | 4 | a0001c0001t0001g0256a0002c0003t0001g0100a0003c0004t0001g0123others(1): Show | 4 | HG00558.hp2 HG01975.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656-459_1656-448d others(14): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(7): Show |
A | 3 | a0002c0003t0001g0133a0003c0004t0002g0129a0004c0010t0001g0270 | 3 | HG03669.hp2 HG03942.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1656-461_1656-448d others(16): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(9): Show |
A | 1 | a0001c0007t0003g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1656-463_1656-448d others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(11): Show |
A | 4 | a0001c0007t0003g0026a0002c0006t0001g0162a0006c0031t0002g0225others(1): Show | 6 | HG00741.hp2 HG01069.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656-465_1656-448d others(20): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(15): Show |
A | 2 | a0001c0007t0003g0223a0024c0026t0003g0222 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1656-469_1656-448d others(24): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(17): Show |
A | 15 | a0001c0001t0001g0244a0003c0004t0002g0036a0003c0038t0002g0066others(12): Show | 38 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1656-471_1656-448d others(26): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441930
|
AGAGAGTG others(19): Show |
A | 1 | a0001c0001t0001g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1656-473_1656-448d others(28): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441930 | ||||||
chr3:46441932
|
AGAGTGT | A | 4 | a0002c0003t0001g0144a0003c0004t0002g0086a0003c0004t0002g0112others(1): Show | 4 | HG00099.hp2 HG00642.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656-455_1656-450d others(8): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(1): Show |
A | 8 | a0001c0002t0003g0199a0002c0003t0001g0018a0002c0003t0001g0117others(5): Show | 11 | HG00280.hp2 HG01074.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1656-457_1656-450d others(10): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(3): Show |
A | 1 | a0003c0004t0002g0141 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1656-459_1656-450d others(12): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(5): Show |
A | 5 | a0001c0020t0001g0267a0003c0004t0002g0095a0003c0004t0002g0127others(2): Show | 5 | HG03209.hp1 HG03516.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1656-461_1656-450d others(14): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(7): Show |
A | 1 | a0019c0050t0007g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1656-463_1656-450d others(16): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(9): Show |
A | 2 | a0001c0014t0001g0023a0007c0008t0001g0079 | 4 | HG02280.hp1 HG02300.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656-465_1656-450d others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(13): Show |
A | 5 | a0004c0023t0001g0040a0007c0008t0001g0003a0007c0008t0001g0009others(2): Show | 17 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1656-469_1656-450d others(22): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441932
|
AGAGTGTG others(15): Show |
A | 1 | a0005c0005t0002g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1656-471_1656-450d others(24): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441932 | ||||||
chr3:46441934
|
A | AGAGAGTG others(1): Show |
1 | a0002c0006t0001g0020 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1656-452_1656-451i others(10): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
A | T | 1 | a0002c0003t0001g0106 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1656-451T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGT | A | 9 | a0001c0002t0001g0045a0001c0002t0001g0174a0001c0002t0001g0198others(6): Show | 10 | HG02040.hp1 HG02071.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1656-455_1656-452d others(6): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGT | A | 11 | a0001c0001t0001g0255a0001c0002t0001g0283a0001c0002t0003g0044others(8): Show | 14 | HG01515.hp1 HG02132.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656-457_1656-452d others(8): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(1): Show |
A | 6 | a0001c0002t0003g0048a0001c0014t0001g0206a0002c0003t0001g0102others(3): Show | 7 | HG01934.hp1 HG02258.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656-459_1656-452d others(10): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(3): Show |
A | 16 | a0001c0002t0001g0050a0001c0002t0001g0215a0001c0002t0003g0190others(13): Show | 21 | HG00639.hp2 HG00738.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1656-461_1656-452d others(12): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(5): Show |
A | 4 | a0001c0007t0001g0224a0001c0007t0001g0231a0004c0010t0001g0278others(1): Show | 4 | HG01978.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656-463_1656-452d others(14): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(7): Show |
A | 5 | a0001c0007t0001g0053a0001c0007t0001g0054a0001c0021t0001g0221others(2): Show | 7 | HG02055.hp2 HG02717.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656-465_1656-452d others(16): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(9): Show |
A | 1 | a0004c0010t0001g0279 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1656-467_1656-452d others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(11): Show |
A | 5 | a0001c0002t0001g0024a0001c0002t0001g0208a0002c0003t0001g0140others(2): Show | 7 | HG01891.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656-469_1656-452d others(20): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(13): Show |
A | 2 | a0007c0008t0001g0082a0017c0045t0002g0176 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1656-471_1656-452d others(22): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441934
|
AGTGTGTG others(23): Show |
A | 1 | a0001c0002t0001g0049 | 2 | NA18612.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1656-481_1656-452d others(32): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441934 | ||||||
chr3:46441936
|
T | A | 1 | a0001c0002t0001g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1656-453A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441936 | ||||||
chr3:46441938
|
T | A | 2 | a0001c0002t0001g0195a0001c0002t0003g0205 | 2 | HG02074.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1656-455A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441938 | ||||||
chr3:46441940
|
T | A | 9 | a0001c0002t0001g0045a0001c0002t0001g0174a0001c0002t0001g0195others(6): Show | 10 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1656-457A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441940 | ||||||
chr3:46441942
|
T | A | 8 | a0001c0002t0001g0045a0001c0002t0003g0046a0001c0002t0003g0047others(5): Show | 11 | HG02040.hp1 HG02074.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.1656-459A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441942 | ||||||
chr3:46441944
|
T | A | 3 | a0001c0002t0003g0205a0001c0014t0001g0206a0008c0018t0001g0069 | 3 | HG01934.hp1 HG02074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1656-461A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441944 | ||||||
chr3:46441946
|
T | A | 4 | a0001c0002t0003g0190a0004c0010t0001g0269a0004c0010t0001g0277others(1): Show | 4 | HG01981.hp1 HG02258.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656-463A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441946 | ||||||
chr3:46441948
|
T | A | 1 | a0001c0007t0001g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1656-465A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441948 | ||||||
chr3:46441954
|
T | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0208a0016c0044t0002g0175 | 5 | HG01891.hp1 HG02647.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1656-471A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441954 | ||||||
chr3:46441956
|
T | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0208 | 4 | HG02647.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656-473A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441956 | ||||||
chr3:46441958
|
T | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0208 | 4 | HG02647.hp2 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656-475A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441958 | ||||||
chr3:46441962
|
T | A | 1 | a0003c0004t0002g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1656-479A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441962 | ||||||
chr3:46441969
|
G | A | 1 | a0005c0005t0002g0152 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1656-486C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441969 | ||||||
chr3:46441971
|
GTGTGTGT others(14): Show |
G | 1 | a0005c0005t0002g0152 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1656-509_1656-489d others(23): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441971 | ||||||
chr3:46441991
|
GC | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 136 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1656-509delG | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46441991 | ||||||
chr3:46442045
|
A | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 143 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1656-562T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442045 | ||||||
chr3:46442084
|
A | T | 37 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0043others(34): Show | 53 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1656-601T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442084 | ||||||
chr3:46442097
|
A | G | 1 | a0004c0024t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1656-614T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442097 | ||||||
chr3:46442139
|
A | T | 15 | a0001c0002t0001g0050a0001c0002t0001g0215a0004c0010t0001g0060others(12): Show | 20 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1656-656T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442139 | ||||||
chr3:46442146
|
A | G | 1 | a0002c0003t0001g0088 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1656-663T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442146 | ||||||
chr3:46442226
|
T | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 177 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1656-743A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442226 | ||||||
chr3:46442258
|
G | C | 1 | a0001c0030t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1656-775C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442258 | ||||||
chr3:46442469
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0246 | 5 | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1655+972G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442469 | ||||||
chr3:46442498
|
GA | G | 5 | a0002c0003t0001g0105a0003c0004t0002g0033a0003c0004t0002g0104others(2): Show | 6 | HG01109.hp1 HG03209.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1655+942delT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442498 | ||||||
chr3:46442631
|
A | AT | 5 | a0001c0001t0001g0218a0005c0005t0002g0151a0006c0009t0002g0016others(2): Show | 8 | HG00423.hp1 HG00673.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1655+809dupA | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442631 | ||||||
chr3:46442650
|
CTTTT | C | 6 | a0004c0023t0001g0040a0008c0018t0001g0068a0008c0018t0001g0069others(3): Show | 7 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1655+787_1655+790d others(6): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442650 | ||||||
chr3:46442770
|
C | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1655+671G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442770 | ||||||
chr3:46442792
|
T | A | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1655+649A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442792 | ||||||
chr3:46442810
|
G | A | 47 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(44): Show | 66 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1655+631C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442810 | ||||||
chr3:46442968
|
G | A | 5 | a0001c0007t0003g0026a0001c0007t0003g0223a0001c0007t0003g0228others(2): Show | 7 | HG01884.hp1 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1655+473C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46442968 | ||||||
chr3:46443008
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 240 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.1655+433G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46443008 | ||||||
chr3:46443058
|
G | A | 6 | a0004c0023t0001g0040a0008c0018t0001g0068a0008c0018t0001g0069others(3): Show | 7 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1655+383C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46443058 | ||||||
chr3:46443060
|
C | T | 1 | a0005c0005t0002g0150 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1655+381G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46443060 | ||||||
chr3:46443082
|
G | A | 21 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(18): Show | 34 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1655+359C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46443082 | ||||||
chr3:46443407
|
T | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(271): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1655+34A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 13/16 | chr3 | 46443407 | ||||||
chr3:46443662
|
G | A | 2 | a0002c0006t0001g0130a0012c0037t0002g0103 | 2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1514-80C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443662 | ||||||
chr3:46443691
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1514-109G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443691 | ||||||
chr3:46443862
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1514-280C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443862 | ||||||
chr3:46443878
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 137 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1514-296C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443878 | ||||||
chr3:46443912
|
C | T | 1 | a0001c0002t0003g0190 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1514-330G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443912 | ||||||
chr3:46443934
|
T | A | 47 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(44): Show | 66 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1514-352A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443934 | ||||||
chr3:46443952
|
C | T | 1 | a0004c0023t0001g0040 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1514-370G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46443952 | ||||||
chr3:46444072
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1514-490C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444072 | ||||||
chr3:46444122
|
G | T | 1 | a0018c0049t0001g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1514-540C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444122 | ||||||
chr3:46444282
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 146 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.1514-700A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444282 | ||||||
chr3:46444383
|
C | T | 4 | a0004c0015t0001g0041a0004c0015t0001g0177a0004c0015t0001g0178others(1): Show | 5 | HG01074.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1514-801G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444383 | ||||||
chr3:46444464
|
G | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1513+817C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444464 | ||||||
chr3:46444468
|
C | CT | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1513+812_1513+813i others(3): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444468 | ||||||
chr3:46444605
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1513+676C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444605 | ||||||
chr3:46444732
|
C | G | 1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1513+549G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444732 | ||||||
chr3:46444738
|
G | A | 21 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(18): Show | 34 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1513+543C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444738 | ||||||
chr3:46444801
|
G | A | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1513+480C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46444801 | ||||||
chr3:46445038
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233 | 5 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1513+243C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46445038 | ||||||
chr3:46445093
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1513+188C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46445093 | ||||||
chr3:46445120
|
G | C | 21 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(18): Show | 34 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1513+161C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 12/16 | chr3 | 46445120 | ||||||
chr3:46445450
|
T | C | 1 | a0001c0002t0003g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1358-14A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445450 | ||||||
chr3:46445512
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1358-76T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445512 | ||||||
chr3:46445519
|
A | G | 2 | a0001c0021t0001g0221a0001c0021t0001g0230 | 2 | HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1358-83T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445519 | ||||||
chr3:46445588
|
C | T | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1358-152G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445588 | ||||||
chr3:46445666
|
G | A | 1 | a0003c0004t0002g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1358-230C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445666 | ||||||
chr3:46445671
|
C | T | 1 | a0001c0020t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1358-235G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445671 | ||||||
chr3:46445762
|
A | G | 45 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(42): Show | 64 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1358-326T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445762 | ||||||
chr3:46445841
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(271): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1358-405T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445841 | ||||||
chr3:46445855
|
T | C | 1 | a0018c0049t0001g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1358-419A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445855 | ||||||
chr3:46445863
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1358-427C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445863 | ||||||
chr3:46445871
|
T | G | 1 | a0001c0007t0001g0052 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358-435A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445871 | ||||||
chr3:46445939
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1357+501C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445939 | ||||||
chr3:46445948
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1357+492G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445948 | ||||||
chr3:46445952
|
G | A | 1 | a0001c0030t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1357+488C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445952 | ||||||
chr3:46445992
|
T | C | 2 | a0004c0012t0001g0017a0004c0012t0001g0072 | 5 | NA18612.hp1 NA18954.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357+448A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46445992 | ||||||
chr3:46446055
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1357+385G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446055 | ||||||
chr3:46446150
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1357+290C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446150 | ||||||
chr3:46446180
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1357+260C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446180 | ||||||
chr3:46446246
|
A | C | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357+194T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446246 | ||||||
chr3:46446259
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 241 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1357+181T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446259 | ||||||
chr3:46446284
|
C | G | 122 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(119): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1357+156G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446284 | ||||||
chr3:46446296
|
TTTGCACC others(10): Show |
T | 122 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(119): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1357+127_1357+143d others(19): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446296 | ||||||
chr3:46446352
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1357+88G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 11/16 | chr3 | 46446352 | ||||||
chr3:46446755
|
G | A | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1304-262C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 10/16 | chr3 | 46446755 | ||||||
chr3:46446777
|
C | A | 1 | a0002c0003t0001g0133 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1304-284G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 10/16 | chr3 | 46446777 | ||||||
chr3:46446893
|
G | A | 2 | a0002c0003t0001g0083a0002c0003t0001g0084 | 2 | HG04184.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1304-400C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 10/16 | chr3 | 46446893 | ||||||
chr3:46446997
|
G | A | 46 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(43): Show | 65 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1303+311C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 10/16 | chr3 | 46446997 | ||||||
chr3:46447025
|
T | C | 1 | a0003c0004t0002g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1303+283A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 10/16 | chr3 | 46447025 | ||||||
chr3:46447445
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0056a0001c0001t0001g0243others(1): Show | 8 | HG00140.hp1 HG01515.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1213-47G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447445 | ||||||
chr3:46447452
|
C | G | 1 | a0008c0018t0001g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1213-54G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447452 | ||||||
chr3:46447524
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 202 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1213-126T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447524 | ||||||
chr3:46447633
|
C | T | 47 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(44): Show | 66 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1213-235G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447633 | ||||||
chr3:46447678
|
C | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | NA19009.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1213-280G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447678 | ||||||
chr3:46447789
|
T | C | 1 | a0024c0026t0003g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1213-391A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447789 | ||||||
chr3:46447879
|
A | C | 2 | a0001c0021t0001g0221a0001c0021t0001g0230 | 2 | HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1213-481T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447879 | ||||||
chr3:46447939
|
T | C | 1 | a0007c0008t0001g0009 | 4 | HG01891.hp2 HG02451.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-541A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46447939 | ||||||
chr3:46448173
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0263 | 7 | HG01123.hp2 HG01952.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+690C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448173 | ||||||
chr3:46448270
|
G | C | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 78 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1212+593C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448270 | ||||||
chr3:46448351
|
A | T | 1 | a0002c0003t0001g0102 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1212+512T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448351 | ||||||
chr3:46448368
|
T | TA | 23 | a0001c0002t0001g0189a0003c0004t0002g0135a0004c0010t0001g0060others(20): Show | 27 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1212+494dupT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448368 | ||||||
chr3:46448368
|
T | TAA | 138 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1212+493_1212+494d others(4): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448368 | ||||||
chr3:46448368
|
TA | T | 5 | a0002c0003t0001g0285a0004c0023t0001g0040a0005c0005t0002g0039others(2): Show | 7 | HG01891.hp1 HG02630.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+494delT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448368 | ||||||
chr3:46448522
|
T | C | 3 | a0006c0013t0002g0051a0006c0013t0002g0211a0006c0013t0002g0216 | 4 | HG00099.hp1 HG01496.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212+341A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448522 | ||||||
chr3:46448587
|
T | G | 4 | a0008c0018t0001g0068a0008c0018t0001g0069a0008c0018t0001g0286others(1): Show | 4 | HG02258.hp2 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212+276A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448587 | ||||||
chr3:46448696
|
C | T | 2 | a0001c0001t0001g0064a0001c0019t0001g0284 | 2 | HG01168.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1212+167G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448696 | ||||||
chr3:46448759
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(189): Show | 290 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.1212+104T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448759 | ||||||
chr3:46448771
|
C | G | 7 | a0004c0056t0001g0077a0007c0008t0001g0003a0007c0008t0001g0009others(4): Show | 18 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1212+92G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 9/16 | chr3 | 46448771 | ||||||
chr3:46449030
|
A | G | 1 | a0004c0047t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1058-13T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449030 | ||||||
chr3:46449116
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233 | 5 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058-99T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449116 | ||||||
chr3:46449490
|
C | A | 1 | a0003c0004t0002g0137 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1057+364G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449490 | ||||||
chr3:46449583
|
A | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 251 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.1057+271T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449583 | ||||||
chr3:46449650
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1057+204C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449650 | ||||||
chr3:46449777
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 120 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1057+77C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449777 | ||||||
chr3:46449800
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 90 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1057+54C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449800 | ||||||
chr3:46449823
|
C | T | 1 | a0001c0030t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1057+31G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 8/16 | chr3 | 46449823 | ||||||
chr3:46450052
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233others(1): Show | 6 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-24A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/16 | chr3 | 46450052 | ||||||
chr3:46450133
|
G | A | 1 | a0001c0002t0003g0213 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.883-105C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/16 | chr3 | 46450133 | ||||||
chr3:46450335
|
G | A | 3 | a0018c0049t0001g0073a0019c0050t0007g0075a0020c0051t0001g0074 | 3 | HG02486.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.882+160C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/16 | chr3 | 46450335 | ||||||
chr3:46450458
|
T | A | 77 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(74): Show | 105 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.882+37A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 7/16 | chr3 | 46450458 | ||||||
chr3:46450899
|
G | A | 1 | a0004c0056t0001g0077 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-226C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46450899 | ||||||
chr3:46450953
|
C | T | 1 | a0004c0023t0001g0040 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.704-280G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46450953 | ||||||
chr3:46451035
|
C | T | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.704-362G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451035 | ||||||
chr3:46451137
|
G | GAAGGGGA others(11): Show |
1 | a0003c0004t0002g0095 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.704-482_704-465dup others(18): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451137 | ||||||
chr3:46451224
|
T | C | 1 | a0001c0002t0003g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.704-551A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451224 | ||||||
chr3:46451231
|
C | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.704-558G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451231 | ||||||
chr3:46451266
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.704-593G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451266 | ||||||
chr3:46451346
|
TACTA | T | 3 | a0018c0049t0001g0073a0019c0050t0007g0075a0020c0051t0001g0074 | 3 | HG02486.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.704-677_704-674del others(4): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451346 | ||||||
chr3:46451382
|
C | T | 3 | a0018c0049t0001g0073a0019c0050t0007g0075a0020c0051t0001g0074 | 3 | HG02486.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.704-709G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451382 | ||||||
chr3:46451401
|
G | C | 8 | a0001c0054t0001g0078a0004c0056t0001g0077a0007c0008t0001g0003others(5): Show | 19 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.704-728C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451401 | ||||||
chr3:46451514
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.704-841G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451514 | ||||||
chr3:46451539
|
T | C | 1 | a0006c0055t0004g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.704-866A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451539 | ||||||
chr3:46451550
|
T | G | 3 | a0018c0049t0001g0073a0019c0050t0007g0075a0020c0051t0001g0074 | 3 | HG02486.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.704-877A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451550 | ||||||
chr3:46451588
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 231 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.704-915A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451588 | ||||||
chr3:46451598
|
T | A | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.704-925A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451598 | ||||||
chr3:46451677
|
C | T | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-1004G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451677 | ||||||
chr3:46451740
|
G | A | 1 | a0002c0003t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.704-1067C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451740 | ||||||
chr3:46451744
|
G | A | 3 | a0004c0016t0001g0157a0004c0016t0001g0158a0005c0005t0002g0005 | 9 | HG00597.hp2 HG02074.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-1071C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451744 | ||||||
chr3:46451841
|
C | A | 1 | a0003c0004t0002g0141 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.704-1168G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451841 | ||||||
chr3:46451938
|
C | T | 77 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(74): Show | 105 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.704-1265G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46451938 | ||||||
chr3:46452036
|
T | C | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.704-1363A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46452036 | ||||||
chr3:46452114
|
G | A | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.704-1441C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46452114 | ||||||
chr3:46452185
|
G | A | 1 | a0001c0019t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.704-1512C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46452185 | ||||||
chr3:46452365
|
G | A | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-1692C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46452365 | ||||||
chr3:46452394
|
C | G | 5 | a0004c0015t0001g0041a0004c0015t0001g0177a0004c0015t0001g0178others(2): Show | 6 | HG01074.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-1721G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46452394 | ||||||
chr3:46452673
|
G | A | 1 | a0002c0006t0001g0038 | 2 | HG02004.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.703+1632C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46452673 | ||||||
chr3:46453032
|
C | T | 1 | a0001c0020t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703+1273G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453032 | ||||||
chr3:46453204
|
G | A | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703+1101C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453204 | ||||||
chr3:46453374
|
G | C | 1 | a0001c0002t0003g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.703+931C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453374 | ||||||
chr3:46453404
|
G | T | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.703+901C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453404 | ||||||
chr3:46453443
|
T | G | 1 | a0002c0006t0001g0167 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.703+862A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453443 | ||||||
chr3:46453472
|
G | T | 1 | a0001c0007t0003g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+833C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453472 | ||||||
chr3:46453743
|
C | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.703+562G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453743 | ||||||
chr3:46453824
|
A | G | 19 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(16): Show | 23 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.703+481T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453824 | ||||||
chr3:46453982
|
A | G | 4 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0220others(1): Show | 7 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+323T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46453982 | ||||||
chr3:46454226
|
C | T | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.703+79G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46454226 | ||||||
chr3:46454236
|
CA | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 122 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.703+68delT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46454236 | ||||||
chr3:46454294
|
C | T | 1 | a0003c0004t0002g0031 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.703+11G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 6/16 | chr3 | 46454294 | ||||||
chr3:46454850
|
C | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 232 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.647+445G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46454850 | ||||||
chr3:46454898
|
C | A | 57 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(54): Show | 81 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.647+397G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46454898 | ||||||
chr3:46454995
|
C | T | 1 | a0001c0020t0001g0267 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.647+300G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46454995 | ||||||
chr3:46455124
|
G | T | 1 | a0003c0004t0002g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.647+171C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46455124 | ||||||
chr3:46455152
|
C | G | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.647+143G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46455152 | ||||||
chr3:46455190
|
G | A | 1 | a0009c0017t0001g0261 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.647+105C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46455190 | ||||||
chr3:46455241
|
G | C | 8 | a0001c0054t0001g0078a0004c0056t0001g0077a0007c0008t0001g0003others(5): Show | 19 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.647+54C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46455241 | ||||||
chr3:46455250
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.647+45G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 5/16 | chr3 | 46455250 | ||||||
chr3:46455670
|
G | A | 1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.499+126C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 4/16 | chr3 | 46455670 | ||||||
chr3:46455732
|
C | T | 1 | a0001c0002t0003g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.499+64G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 4/16 | chr3 | 46455732 | ||||||
chr3:46456001
|
G | A | 17 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(14): Show | 24 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.317-23C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 3/16 | chr3 | 46456001 | ||||||
chr3:46456081
|
C | T | 3 | a0008c0018t0001g0068a0008c0018t0001g0069a0008c0018t0001g0286 | 3 | HG02258.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.317-103G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 3/16 | chr3 | 46456081 | ||||||
chr3:46456100
|
G | A | 1 | a0001c0002t0001g0022 | 3 | HG00639.hp1 HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.317-122C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 3/16 | chr3 | 46456100 | ||||||
chr3:46456115
|
G | A | 3 | a0008c0018t0001g0068a0008c0018t0001g0069a0008c0018t0001g0286 | 3 | HG02258.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.317-137C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 3/16 | chr3 | 46456115 | ||||||
chr3:46456185
|
A | G | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.316+105T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 3/16 | chr3 | 46456185 | ||||||
chr3:46456233
|
C | G | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.316+57G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 3/16 | chr3 | 46456233 | ||||||
chr3:46456510
|
C | T | 1 | a0005c0005t0002g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.208-112G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456510 | ||||||
chr3:46456522
|
T | C | 1 | a0003c0004t0002g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.208-124A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456522 | ||||||
chr3:46456750
|
A | G | 1 | a0003c0004t0002g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.208-352T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456750 | ||||||
chr3:46456771
|
C | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 257 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.208-373G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456771 | ||||||
chr3:46456771
|
C | G | 3 | a0018c0049t0001g0073a0019c0050t0007g0075a0020c0051t0001g0074 | 3 | HG02486.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.208-373G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456771 | ||||||
chr3:46456870
|
G | T | 7 | a0001c0002t0001g0022a0001c0002t0001g0182a0001c0002t0001g0183others(4): Show | 12 | HG00639.hp1 HG00735.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-472C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456870 | ||||||
chr3:46456958
|
C | T | 70 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(67): Show | 105 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.208-560G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456958 | ||||||
chr3:46456966
|
C | T | 8 | a0001c0054t0001g0078a0004c0056t0001g0077a0007c0008t0001g0003others(5): Show | 19 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.208-568G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456966 | ||||||
chr3:46456973
|
C | T | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.208-575G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456973 | ||||||
chr3:46456974
|
A | G | 60 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(57): Show | 84 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.208-576T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456974 | ||||||
chr3:46456982
|
T | C | 62 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(59): Show | 86 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.208-584A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456982 | ||||||
chr3:46456991
|
C | T | 70 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(67): Show | 105 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.208-593G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46456991 | ||||||
chr3:46457000
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0235 | 4 | HG02080.hp2 NA18944.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-602A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457000 | ||||||
chr3:46457321
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.208-923C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457321 | ||||||
chr3:46457324
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233 | 5 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-926A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457324 | ||||||
chr3:46457331
|
T | A | 2 | a0019c0050t0007g0075a0020c0051t0001g0074 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.208-933A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457331 | ||||||
chr3:46457333
|
A | AT | 4 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0220others(1): Show | 7 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-936dupA | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457333 | ||||||
chr3:46457375
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(187): Show | 299 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.208-977A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457375 | ||||||
chr3:46457387
|
T | A | 1 | a0008c0018t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.208-989A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457387 | ||||||
chr3:46457426
|
T | C | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.208-1028A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457426 | ||||||
chr3:46457485
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 127 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.208-1087G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457485 | ||||||
chr3:46457501
|
C | A | 1 | a0002c0003t0001g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.208-1103G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457501 | ||||||
chr3:46457510
|
C | T | 1 | a0001c0007t0001g0220 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.208-1112G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457510 | ||||||
chr3:46457558
|
G | A | 17 | a0001c0054t0001g0078a0004c0048t0001g0287a0004c0056t0001g0077others(14): Show | 28 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.208-1160C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457558 | ||||||
chr3:46457583
|
C | T | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.208-1185G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457583 | ||||||
chr3:46457615
|
A | G | 1 | a0003c0004t0002g0092 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-1217T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457615 | ||||||
chr3:46457621
|
T | A | 1 | a0001c0001t0001g0263 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.208-1223A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457621 | ||||||
chr3:46457682
|
C | T | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.208-1284G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457682 | ||||||
chr3:46457856
|
C | T | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.208-1458G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457856 | ||||||
chr3:46457913
|
G | A | 21 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(18): Show | 25 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.208-1515C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457913 | ||||||
chr3:46457944
|
A | AT | 92 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(89): Show | 133 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.208-1547dupA | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457944 | ||||||
chr3:46457944
|
AT | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233others(22): Show | 34 | HG00438.hp1 HG01069.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.208-1547delA | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457944 | ||||||
chr3:46457944
|
ATT | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 119 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.208-1548_208-1547d others(4): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457944 | ||||||
chr3:46457982
|
C | T | 6 | a0002c0003t0001g0018a0002c0003t0001g0019a0002c0003t0001g0030others(3): Show | 11 | HG00621.hp2 NA18946.hp1 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-1584G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46457982 | ||||||
chr3:46458054
|
G | A | 1 | a0006c0013t0002g0216 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.207+1602C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458054 | ||||||
chr3:46458079
|
C | T | 1 | a0004c0010t0001g0273 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.207+1577G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458079 | ||||||
chr3:46458229
|
G | T | 3 | a0004c0023t0001g0040a0016c0044t0002g0175a0017c0045t0002g0176 | 4 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1427C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458229 | ||||||
chr3:46458473
|
T | TTTTGTGG others(1): Show |
55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.207+1175_207+1182d others(10): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458473 | ||||||
chr3:46458554
|
T | A | 1 | a0002c0003t0001g0144 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.207+1102A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458554 | ||||||
chr3:46458614
|
G | A | 1 | a0003c0004t0002g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.207+1042C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458614 | ||||||
chr3:46458637
|
T | G | 19 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(16): Show | 23 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.207+1019A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458637 | ||||||
chr3:46458798
|
C | G | 10 | a0001c0054t0001g0078a0004c0056t0001g0077a0006c0055t0004g0063others(7): Show | 21 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.207+858G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458798 | ||||||
chr3:46458826
|
C | T | 1 | a0003c0004t0002g0087 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.207+830G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458826 | ||||||
chr3:46458864
|
G | A | 9 | a0001c0054t0001g0078a0006c0055t0004g0063a0007c0008t0001g0003others(6): Show | 20 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.207+792C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458864 | ||||||
chr3:46458865
|
C | T | 1 | a0006c0055t0004g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.207+791G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458865 | ||||||
chr3:46458874
|
A | C | 4 | a0004c0048t0001g0287a0008c0018t0001g0068a0008c0018t0001g0069others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+782T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458874 | ||||||
chr3:46458968
|
C | T | 19 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(16): Show | 23 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.207+688G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458968 | ||||||
chr3:46458991
|
A | C | 1 | a0006c0013t0002g0217 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.207+665T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46458991 | ||||||
chr3:46459003
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.207+653G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459003 | ||||||
chr3:46459065
|
G | A | 1 | a0001c0007t0001g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+591C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459065 | ||||||
chr3:46459069
|
G | T | 17 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0053others(14): Show | 24 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.207+587C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459069 | ||||||
chr3:46459222
|
A | T | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.207+434T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459222 | ||||||
chr3:46459226
|
C | A | 8 | a0001c0054t0001g0078a0006c0055t0004g0063a0007c0008t0001g0003others(5): Show | 19 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.207+430G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459226 | ||||||
chr3:46459255
|
T | G | 1 | a0006c0013t0002g0217 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.207+401A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459255 | ||||||
chr3:46459266
|
T | A | 1 | a0011c0035t0002g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.207+390A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459266 | ||||||
chr3:46459398
|
A | G | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.207+258T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459398 | ||||||
chr3:46459405
|
G | A | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.207+251C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459405 | ||||||
chr3:46459434
|
G | C | 1 | a0003c0004t0002g0146 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.207+222C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459434 | ||||||
chr3:46459488
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 91 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.207+168G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459488 | ||||||
chr3:46459521
|
G | A | 1 | a0003c0004t0002g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.207+135C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459521 | ||||||
chr3:46459548
|
C | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233 | 5 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+108G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459548 | ||||||
chr3:46459610
|
C | A | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.207+46G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459610 | ||||||
chr3:46459634
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0059a0001c0001t0001g0235others(1): Show | 7 | HG02080.hp2 NA18944.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+22G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459634 | ||||||
chr3:46459642
|
C | T | 1 | a0003c0004t0002g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.207+14G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 2/16 | chr3 | 46459642 | ||||||
chr3:46459845
|
G | A | 4 | a0004c0048t0001g0287a0008c0018t0001g0068a0008c0018t0001g0069others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-26C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46459845 | ||||||
chr3:46459971
|
G | A | 2 | a0001c0020t0001g0267a0001c0020t0001g0268 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.44-152C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46459971 | ||||||
chr3:46459996
|
G | A | 1 | a0003c0041t0002g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.44-177C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46459996 | ||||||
chr3:46460061
|
A | T | 4 | a0004c0012t0001g0017a0004c0012t0001g0072a0004c0012t0001g0271others(1): Show | 7 | NA18612.hp1 NA18954.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-242T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460061 | ||||||
chr3:46460128
|
T | G | 1 | a0004c0024t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.44-309A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460128 | ||||||
chr3:46460129
|
T | A | 1 | a0004c0024t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.44-310A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460129 | ||||||
chr3:46460272
|
G | A | 2 | a0002c0006t0001g0162a0003c0004t0002g0163 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.44-453C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460272 | ||||||
chr3:46460279
|
C | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(156): Show | 244 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.44-460G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460279 | ||||||
chr3:46460348
|
C | A | 1 | a0021c0027t0003g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.44-529G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460348 | ||||||
chr3:46460352
|
G | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 262 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.44-533C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460352 | ||||||
chr3:46460417
|
C | T | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-598G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460417 | ||||||
chr3:46460441
|
C | T | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.44-622G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460441 | ||||||
chr3:46460531
|
T | TA | 2 | a0001c0001t0001g0059a0004c0016t0001g0264 | 3 | NA18962.hp1 NA18966.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.44-713dupT | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460531 | ||||||
chr3:46460565
|
C | G | 1 | a0022c0032t0003g0181 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.44-746G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460565 | ||||||
chr3:46460741
|
G | A | 1 | a0002c0006t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.44-922C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460741 | ||||||
chr3:46460797
|
ATCT | A | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.44-981_44-979delAG others(1): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460797 | ||||||
chr3:46460800
|
T | A | 1 | a0001c0001t0001g0265 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.44-981A>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460800 | ||||||
chr3:46460833
|
T | G | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-1014A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460833 | ||||||
chr3:46460991
|
C | T | 8 | a0001c0054t0001g0078a0006c0055t0004g0063a0007c0008t0001g0003others(5): Show | 19 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-1172G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460991 | ||||||
chr3:46460992
|
G | A | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.44-1173C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46460992 | ||||||
chr3:46461329
|
C | T | 2 | a0002c0003t0001g0083a0002c0003t0001g0084 | 2 | HG04184.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.44-1510G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461329 | ||||||
chr3:46461330
|
C | T | 1 | a0002c0003t0001g0018 | 3 | NA19004.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.44-1511G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461330 | ||||||
chr3:46461344
|
T | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 249 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.44-1525A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461344 | ||||||
chr3:46461656
|
C | A | 1 | a0005c0005t0002g0164 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.44-1837G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461656 | ||||||
chr3:46461679
|
G | A | 1 | a0004c0024t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44-1860C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461679 | ||||||
chr3:46461724
|
G | A | 16 | a0004c0010t0001g0060a0004c0010t0001g0269a0004c0010t0001g0273others(13): Show | 20 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.44-1905C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461724 | ||||||
chr3:46461766
|
A | AT | 160 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 245 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.44-1948dupA | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461766 | ||||||
chr3:46461780
|
G | A | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.44-1961C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461780 | ||||||
chr3:46461947
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233 | 5 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-2128C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46461947 | ||||||
chr3:46462008
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 245 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.44-2189T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462008 | ||||||
chr3:46462219
|
C | T | 22 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0233others(19): Show | 31 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.44-2400G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462219 | ||||||
chr3:46462263
|
A | G | 55 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(52): Show | 79 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.44-2444T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462263 | ||||||
chr3:46462302
|
A | G | 4 | a0001c0007t0001g0025a0001c0007t0001g0052a0001c0007t0001g0220others(1): Show | 7 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-2483T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462302 | ||||||
chr3:46462313
|
AACAAATA others(13): Show |
A | 3 | a0002c0006t0001g0168a0002c0006t0001g0170a0003c0004t0002g0169 | 3 | HG00738.hp1 HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.43+2492_44-2495del others(20): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462313 | ||||||
chr3:46462340
|
G | A | 7 | a0001c0054t0001g0078a0007c0008t0001g0003a0007c0008t0001g0009others(4): Show | 18 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.43+2485C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462340 | ||||||
chr3:46462359
|
C | T | 3 | a0018c0049t0001g0073a0019c0050t0007g0075a0020c0051t0001g0074 | 3 | HG02486.hp1 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.43+2466G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462359 | ||||||
chr3:46462416
|
T | G | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+2409A>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462416 | ||||||
chr3:46462736
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 167 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.43+2089T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462736 | ||||||
chr3:46462826
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 264 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.43+1999T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462826 | ||||||
chr3:46462860
|
A | AAC | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1964_43+1965ins others(2): Show |
LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462860 | ||||||
chr3:46462861
|
G | C | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1964C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462861 | ||||||
chr3:46462862
|
A | C | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1963T>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462862 | ||||||
chr3:46462864
|
A | G | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1961T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462864 | ||||||
chr3:46462865
|
G | C | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1960C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462865 | ||||||
chr3:46462867
|
A | T | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1958T>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462867 | ||||||
chr3:46462868
|
A | G | 56 | a0001c0002t0001g0006a0001c0002t0001g0022a0001c0002t0001g0024others(53): Show | 80 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.43+1957T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462868 | ||||||
chr3:46462899
|
G | A | 6 | a0002c0006t0001g0165a0002c0006t0001g0166a0002c0006t0001g0167others(3): Show | 6 | HG00738.hp1 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+1926C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46462899 | ||||||
chr3:46463013
|
C | G | 1 | a0004c0010t0001g0269 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.43+1812G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463013 | ||||||
chr3:46463041
|
G | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(88): Show | 138 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.43+1784C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463041 | ||||||
chr3:46463236
|
A | G | 18 | a0004c0010t0001g0060a0004c0010t0001g0071a0004c0010t0001g0269others(15): Show | 22 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+1589T>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463236 | ||||||
chr3:46463416
|
C | T | 17 | a0001c0001t0001g0067a0001c0002t0001g0174a0001c0014t0001g0173others(14): Show | 19 | HG01074.hp1 HG01891.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.43+1409G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463416 | ||||||
chr3:46463759
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43+1066G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463759 | ||||||
chr3:46463776
|
G | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 209 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.43+1049C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463776 | ||||||
chr3:46463810
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.43+1015G>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463810 | ||||||
chr3:46463825
|
G | C | 20 | a0001c0002t0001g0283a0001c0020t0001g0267a0001c0020t0001g0268others(17): Show | 24 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+1000C>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463825 | ||||||
chr3:46463834
|
C | T | 1 | a0004c0010t0001g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.43+991G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463834 | ||||||
chr3:46463886
|
G | A | 1 | a0001c0019t0001g0284 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.43+939C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463886 | ||||||
chr3:46463926
|
C | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0070a0004c0024t0001g0062others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+899G>C | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46463926 | ||||||
chr3:46464067
|
T | C | 1 | a0002c0003t0001g0285 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.43+758A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464067 | ||||||
chr3:46464080
|
T | C | 1 | a0008c0018t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.43+745A>G | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464080 | ||||||
chr3:46464114
|
C | T | 1 | a0003c0038t0002g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.43+711G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464114 | ||||||
chr3:46464155
|
G | T | 2 | a0001c0001t0001g0064a0006c0029t0002g0065 | 2 | HG01168.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.43+670C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464155 | ||||||
chr3:46464286
|
C | T | 2 | a0004c0024t0001g0062a0006c0055t0004g0063 | 2 | HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.43+539G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464286 | ||||||
chr3:46464464
|
G | A | 1 | a0004c0048t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.43+361C>T | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464464 | ||||||
chr3:46464701
|
G | T | 1 | a0004c0047t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43+124C>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464701 | ||||||
chr3:46464786
|
C | T | 1 | a0006c0009t0002g0029 | 2 | HG00558.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.43+39G>A | LTF | ENSG00000012223.13 | transcript | ENST00000231751.9 | protein_coding | 1/16 | chr3 | 46464786 |