geneid | 7018 |
---|---|
ensemblid | ENSG00000091513.16 |
hgncid | 11740 |
symbol | TF |
name | transferrin |
refseq_nuc | NM_001063.4 |
refseq_prot | NP_001054.2 |
ensembl_nuc | ENST00000402696.9 |
ensembl_prot | ENSP00000385834.3 |
mane_status | MANE Select |
chr | chr3 |
start | 133746393 |
end | 133796641 |
strand | + |
ver | v1.2 |
region | chr3:133746393-133796641 |
region5000 | chr3:133741393-133801641 |
regionname0 | TF_chr3_133746393_133796641 |
regionname5000 | TF_chr3_133741393_133801641 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 698 | 304 | 79 | 60 | 118 | 15 | 31 | 94 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002 | 0/0 | 698 | 70 | 9 | 10 | 40 | 1 | 10 | 31 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003 | 0/0 | 698 | 12 | 0 | 5 | 0 | 2 | 5 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0004 | 0/0 | 698 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0005 | 0/0 | 698 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006 | 1/0 | 698 | 4 | 0 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0007 | 0/0 | 698 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0008 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2097 | 107 | 7 | 20 | 58 | 5 | 17 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0002 | 0/0 | 2097 | 64 | 9 | 10 | 38 | 1 | 6 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0003 | 0/0 | 2097 | 57 | 17 | 20 | 10 | 4 | 6 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0004 | 0/1 | 2097 | 53 | 2 | 8 | 33 | 3 | 6 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0005 | 0/0 | 2097 | 42 | 23 | 9 | 7 | 3 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0006 | 0/0 | 2097 | 18 | 17 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0007 | 0/0 | 2097 | 12 | 0 | 0 | 10 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0008 | 0/0 | 2097 | 11 | 0 | 5 | 0 | 2 | 4 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0009 | 0/0 | 2097 | 8 | 8 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0010 | 0/0 | 2097 | 5 | 0 | 0 | 5 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0011 | 0/0 | 2097 | 5 | 5 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0012 | 0/0 | 2097 | 3 | 0 | 0 | 0 | 0 | 3 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0013 | 0/0 | 2097 | 3 | 0 | 3 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0014 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0015 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0016 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0017 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0018 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0019 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0020 | 1/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0021 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0022 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0023 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0024 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
c0025 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 16743 | 14 | 0 | 1 | 10 | 0 | 3 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0002 | 0/0 | 16743 | 11 | 0 | 3 | 7 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0003 | 0/0 | 18062 | 9 | 0 | 1 | 8 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0004 | 0/0 | 18070 | 9 | 0 | 0 | 9 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0005 | 0/0 | 16745 | 8 | 0 | 1 | 4 | 2 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0006 | 0/0 | 16743 | 8 | 0 | 0 | 6 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0007 | 0/0 | 16743 | 6 | 0 | 2 | 0 | 2 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0008 | 0/0 | 16744 | 5 | 0 | 0 | 3 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0009 | 0/0 | 18062 | 4 | 0 | 2 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0010 | 0/0 | 18064 | 4 | 0 | 0 | 4 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0011 | 0/0 | 16745 | 4 | 1 | 1 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0012 | 0/0 | 18069 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0013 | 0/0 | 18063 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0014 | 0/0 | 18061 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0015 | 0/0 | 18061 | 3 | 1 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0016 | 0/0 | 18081 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0017 | 0/0 | 18067 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0018 | 0/1 | 18070 | 3 | 0 | 1 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0019 | 0/0 | 18069 | 3 | 0 | 1 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0020 | 0/0 | 16743 | 3 | 0 | 1 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0021 | 0/0 | 18066 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0022 | 0/0 | 18067 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0023 | 0/0 | 18024 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0024 | 0/0 | 18171 | 3 | 0 | 3 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0025 | 0/0 | 18172 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0026 | 0/0 | 16745 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0027 | 0/0 | 18070 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0028 | 0/0 | 18073 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0029 | 0/0 | 18071 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0030 | 0/0 | 18060 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0031 | 0/0 | 18063 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0032 | 0/0 | 18062 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0033 | 0/0 | 18062 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0034 | 0/0 | 18064 | 2 | 0 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0035 | 0/0 | 18072 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0036 | 0/0 | 18065 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0037 | 0/0 | 18067 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0038 | 0/0 | 18068 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0039 | 0/0 | 18070 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0040 | 0/0 | 18071 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0041 | 0/0 | 18019 | 2 | 0 | 0 | 0 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0042 | 0/0 | 18018 | 2 | 0 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0043 | 0/0 | 18061 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0044 | 0/0 | 18011 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0045 | 0/0 | 18060 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0046 | 0/0 | 18067 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0047 | 0/0 | 18019 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0048 | 0/0 | 18172 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0049 | 0/0 | 17749 | 2 | 0 | 1 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0050 | 0/0 | 16745 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0051 | 0/0 | 16744 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0052 | 0/0 | 16744 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0053 | 0/0 | 16745 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0054 | 0/0 | 16745 | 2 | 0 | 0 | 0 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0055 | 0/0 | 16744 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0056 | 0/0 | 18069 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0057 | 0/0 | 16742 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0058 | 0/0 | 16747 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0059 | 0/0 | 18069 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0060 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0061 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0062 | 0/0 | 18068 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0063 | 0/0 | 18066 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0064 | 0/0 | 18065 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0065 | 0/0 | 18067 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0066 | 0/0 | 18057 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0067 | 1/0 | 18070 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0068 | 0/0 | 18070 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0069 | 0/0 | 18071 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0070 | 0/0 | 18071 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0071 | 0/0 | 18063 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0072 | 0/0 | 18071 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0073 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0074 | 0/0 | 18073 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0075 | 0/0 | 18074 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0076 | 0/0 | 18072 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0077 | 0/0 | 18076 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0078 | 0/0 | 18072 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0079 | 0/0 | 18070 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0080 | 0/0 | 18070 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0081 | 0/0 | 18070 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0082 | 0/0 | 18072 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0083 | 0/0 | 18068 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0084 | 0/0 | 18071 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0085 | 0/0 | 18070 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0086 | 0/0 | 18061 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0087 | 0/0 | 18021 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0088 | 0/0 | 18014 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0089 | 0/0 | 18063 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0090 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0091 | 0/0 | 18064 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0092 | 0/0 | 18064 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0093 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0094 | 0/0 | 18063 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0095 | 0/0 | 18063 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0096 | 0/0 | 18013 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0097 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0098 | 0/0 | 18061 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0099 | 0/0 | 18061 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0100 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0101 | 0/0 | 16745 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0102 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0103 | 0/0 | 18061 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0104 | 0/0 | 18061 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0105 | 0/0 | 18061 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0106 | 0/0 | 18061 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0107 | 0/0 | 18060 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0108 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0109 | 0/0 | 18060 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0110 | 0/0 | 18061 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0111 | 0/0 | 18060 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0112 | 0/0 | 18071 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0113 | 0/0 | 18065 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0114 | 0/0 | 18073 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0115 | 0/0 | 18074 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0116 | 0/0 | 18074 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0117 | 0/0 | 18065 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0118 | 0/0 | 18063 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0119 | 0/0 | 18064 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0120 | 0/0 | 18061 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0121 | 0/0 | 17749 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0122 | 0/0 | 16745 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0123 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0124 | 0/0 | 16742 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0125 | 0/0 | 16743 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0126 | 0/0 | 16743 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0127 | 0/0 | 18064 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0128 | 0/0 | 18081 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0129 | 0/0 | 18082 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0130 | 0/0 | 18083 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0131 | 0/0 | 18081 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0132 | 0/0 | 18082 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0133 | 0/0 | 18081 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0134 | 0/0 | 18081 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0135 | 0/0 | 18082 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0136 | 0/0 | 18077 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0137 | 0/0 | 18078 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0138 | 0/0 | 18072 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0139 | 0/0 | 18171 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0140 | 0/0 | 18067 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0141 | 0/0 | 18066 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0142 | 0/0 | 18070 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0143 | 0/0 | 18068 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0144 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0145 | 0/0 | 18071 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0146 | 0/0 | 18070 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0147 | 0/0 | 18072 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0148 | 0/0 | 18070 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0149 | 0/0 | 18072 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0150 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0151 | 0/0 | 18070 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0152 | 0/0 | 18068 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0153 | 0/0 | 18069 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0154 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0155 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0156 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0157 | 0/0 | 18074 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0158 | 0/0 | 18022 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0159 | 0/0 | 18021 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0160 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0161 | 0/0 | 18069 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0162 | 0/0 | 18071 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0163 | 0/0 | 18072 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0164 | 0/0 | 18073 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0165 | 0/0 | 18070 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0166 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0167 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0168 | 0/0 | 18070 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0169 | 0/0 | 18070 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0170 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0171 | 0/0 | 16741 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0172 | 0/0 | 18071 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0173 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0174 | 0/0 | 18060 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0175 | 0/0 | 18019 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0176 | 0/0 | 18018 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0177 | 0/0 | 18018 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0178 | 0/0 | 17934 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0179 | 0/0 | 17933 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0180 | 0/0 | 18076 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0181 | 0/0 | 18026 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0182 | 0/0 | 18071 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0183 | 0/0 | 18061 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0184 | 0/0 | 18070 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0185 | 0/0 | 18010 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0186 | 0/0 | 18060 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0187 | 0/0 | 18060 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0188 | 0/0 | 18064 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0189 | 0/0 | 18016 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0190 | 0/0 | 18019 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0191 | 0/0 | 18303 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0192 | 0/0 | 18076 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0193 | 0/0 | 18172 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0194 | 0/0 | 18173 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0195 | 0/0 | 18074 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0196 | 0/0 | 18074 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0197 | 0/0 | 18171 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0198 | 0/0 | 18065 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0199 | 0/0 | 18058 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0200 | 0/0 | 18074 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0201 | 0/0 | 18172 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0202 | 0/0 | 18171 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0203 | 0/0 | 18269 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0204 | 0/0 | 18072 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0205 | 0/0 | 18073 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0206 | 0/0 | 18063 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0207 | 0/0 | 18064 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0208 | 0/0 | 18063 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0209 | 0/0 | 16743 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0210 | 0/0 | 18172 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0211 | 0/0 | 18168 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0212 | 0/0 | 18070 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0213 | 0/0 | 18072 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0214 | 0/0 | 18067 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0215 | 0/0 | 16746 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0216 | 0/0 | 16745 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0217 | 0/0 | 16744 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0218 | 0/0 | 16745 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0219 | 0/0 | 16745 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0220 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0221 | 0/0 | 16745 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0222 | 0/0 | 16746 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0223 | 0/0 | 16744 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0224 | 0/0 | 16752 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0225 | 0/0 | 16744 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0226 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0227 | 0/0 | 16743 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0228 | 0/0 | 16744 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0229 | 0/0 | 16741 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0230 | 0/0 | 16745 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0231 | 0/0 | 16746 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0232 | 0/0 | 16746 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0233 | 0/0 | 16743 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0234 | 0/0 | 16742 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0235 | 0/0 | 16742 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0236 | 0/0 | 16743 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0237 | 0/0 | 16749 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0238 | 0/0 | 16742 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0239 | 0/0 | 16744 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0240 | 0/0 | 16745 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0241 | 0/0 | 16742 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0242 | 0/0 | 16744 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0243 | 0/0 | 16743 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0244 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0245 | 0/0 | 16741 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0246 | 0/0 | 16742 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0247 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0248 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0249 | 0/0 | 18058 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0250 | 0/0 | 16741 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0251 | 0/0 | 16742 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0252 | 0/0 | 18070 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0253 | 0/0 | 18071 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0254 | 0/0 | 16744 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0255 | 0/0 | 16745 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0256 | 0/0 | 16746 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0257 | 0/0 | 16743 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0258 | 0/0 | 16744 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0259 | 0/0 | 16743 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0260 | 0/0 | 18070 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0261 | 0/0 | 18060 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0262 | 0/0 | 18066 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0263 | 0/0 | 16745 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0264 | 0/0 | 18083 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0265 | 0/0 | 18074 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0266 | 0/0 | 18073 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0267 | 0/0 | 18073 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
t0268 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 18 | 0 | 1 | 12 | 2 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0002 | 0/0 | 17 | 0 | 2 | 11 | 0 | 4 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0003 | 0/0 | 9 | 1 | 1 | 5 | 0 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0004 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0007 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0008 | 0/0 | 7 | 2 | 2 | 1 | 0 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0010 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0011 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0014 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0015 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0016 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0017 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0021 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0026 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2097 | 107 | 7 | 20 | 58 | 5 | 17 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003 | 0/0 | 2097 | 57 | 17 | 20 | 10 | 4 | 6 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004 | 0/1 | 2097 | 53 | 2 | 8 | 33 | 3 | 6 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005 | 0/0 | 2097 | 42 | 23 | 9 | 7 | 3 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006 | 0/0 | 2097 | 18 | 17 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007 | 0/0 | 2097 | 12 | 0 | 0 | 10 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009 | 0/0 | 2097 | 8 | 8 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0014 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0015 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0017 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0018 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0024 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002 | 0/0 | 2097 | 64 | 9 | 10 | 38 | 1 | 6 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0012 | 0/0 | 2097 | 3 | 0 | 0 | 0 | 0 | 3 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0019 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0021 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0022 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008 | 0/0 | 2097 | 11 | 0 | 5 | 0 | 2 | 4 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0016 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0004c0010 | 0/0 | 2097 | 5 | 0 | 0 | 5 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0005c0011 | 0/0 | 2097 | 5 | 5 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006c0013 | 0/0 | 2097 | 3 | 0 | 3 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006c0020 | 1/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0007c0025 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0008c0023 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 18839 | 12 | 0 | 1 | 9 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0002 | 0/0 | 18839 | 10 | 0 | 3 | 6 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0005 | 0/0 | 18841 | 7 | 0 | 1 | 3 | 2 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0006 | 0/0 | 18839 | 7 | 0 | 0 | 6 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0008 | 0/0 | 18840 | 3 | 0 | 0 | 2 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0011 | 0/0 | 18841 | 3 | 1 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0025 | 0/0 | 20268 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0026 | 0/0 | 18841 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0049 | 0/0 | 19845 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0050 | 0/0 | 18841 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0051 | 0/0 | 18840 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0052 | 0/0 | 18840 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0053 | 0/0 | 18841 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0054 | 0/0 | 18841 | 2 | 0 | 0 | 0 | 0 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0055 | 0/0 | 18840 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0057 | 0/0 | 18838 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0058 | 0/0 | 18843 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0215 | 0/0 | 18842 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0216 | 0/0 | 18841 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0217 | 0/0 | 18840 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0218 | 0/0 | 18841 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0219 | 0/0 | 18841 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0220 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0221 | 0/0 | 18841 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0222 | 0/0 | 18842 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0223 | 0/0 | 18840 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0225 | 0/0 | 18840 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0226 | 0/0 | 20165 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0227 | 0/0 | 18839 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0228 | 0/0 | 18840 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0229 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0230 | 0/0 | 18841 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0231 | 0/0 | 18842 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0232 | 0/0 | 18842 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0233 | 0/0 | 18839 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0234 | 0/0 | 18838 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0235 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0236 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0238 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0239 | 0/0 | 18840 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0240 | 0/0 | 18841 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0241 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0242 | 0/0 | 18840 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0243 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0244 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0245 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0246 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0247 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0249 | 0/0 | 20154 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0250 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0251 | 0/0 | 18838 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0252 | 0/0 | 20166 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0253 | 0/0 | 20167 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0254 | 0/0 | 18840 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0255 | 0/0 | 18841 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0256 | 0/0 | 18842 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0257 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0258 | 0/0 | 18840 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0259 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0260 | 0/0 | 20166 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0261 | 0/0 | 20156 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0262 | 0/0 | 20162 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0001t0263 | 0/0 | 18841 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0007 | 0/0 | 18839 | 6 | 0 | 2 | 0 | 2 | 2 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0010 | 0/0 | 20160 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0011 | 0/0 | 18841 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0023 | 0/0 | 20120 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0024 | 0/0 | 20267 | 3 | 0 | 3 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0025 | 0/0 | 20268 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0034 | 0/0 | 20160 | 2 | 0 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0039 | 0/0 | 20166 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0048 | 0/0 | 20268 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0049 | 0/0 | 19845 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0055 | 0/0 | 18840 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0056 | 0/0 | 20165 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0057 | 0/0 | 18838 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0070 | 0/0 | 20167 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0112 | 0/0 | 20167 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0115 | 0/0 | 20170 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0116 | 0/0 | 20170 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0118 | 0/0 | 20159 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0119 | 0/0 | 20160 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0120 | 0/0 | 20157 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0121 | 0/0 | 19845 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0122 | 0/0 | 18841 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0123 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0124 | 0/0 | 18838 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0125 | 0/0 | 18839 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0126 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0127 | 0/0 | 20160 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0138 | 0/0 | 20168 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0139 | 0/0 | 20267 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0147 | 0/0 | 20168 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0148 | 0/0 | 20166 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0150 | 0/0 | 20165 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0181 | 0/0 | 20122 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0182 | 0/0 | 20167 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0193 | 0/0 | 20268 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0194 | 0/0 | 20269 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0201 | 0/0 | 20268 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0202 | 0/0 | 20267 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0203 | 0/0 | 20365 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0210 | 0/0 | 20268 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0211 | 0/0 | 20264 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0212 | 0/0 | 20166 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0224 | 0/0 | 18848 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0237 | 0/0 | 18845 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0248 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0003t0265 | 0/0 | 20170 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0001 | 0/0 | 18839 | 2 | 0 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0002 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0004 | 0/0 | 20166 | 8 | 0 | 0 | 8 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0005 | 0/0 | 18841 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0006 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0008 | 0/0 | 18840 | 2 | 0 | 0 | 1 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0018 | 0/1 | 20166 | 3 | 0 | 1 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0019 | 0/0 | 20165 | 3 | 0 | 1 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0020 | 0/0 | 18839 | 3 | 0 | 1 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0035 | 0/0 | 20168 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0036 | 0/0 | 20161 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0039 | 0/0 | 20166 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0040 | 0/0 | 20167 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0053 | 0/0 | 18841 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0141 | 0/0 | 20162 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0142 | 0/0 | 20166 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0145 | 0/0 | 20167 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0155 | 0/0 | 20163 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0157 | 0/0 | 20170 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0158 | 0/0 | 20118 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0159 | 0/0 | 20117 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0160 | 0/0 | 20165 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0161 | 0/0 | 20165 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0162 | 0/0 | 20167 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0163 | 0/0 | 20168 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0164 | 0/0 | 20169 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0165 | 0/0 | 20166 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0166 | 0/0 | 20164 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0168 | 0/0 | 20166 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0170 | 0/0 | 18839 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0171 | 0/0 | 18837 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0172 | 0/0 | 20167 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0204 | 0/0 | 20168 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0205 | 0/0 | 20169 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0213 | 0/0 | 20168 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0004t0266 | 0/0 | 20169 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0012 | 0/0 | 20165 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0016 | 0/0 | 20177 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0027 | 0/0 | 20166 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0028 | 0/0 | 20169 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0029 | 0/0 | 20167 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0060 | 0/0 | 20165 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0061 | 0/0 | 20165 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0062 | 0/0 | 20164 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0063 | 0/0 | 20162 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0064 | 0/0 | 20161 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0065 | 0/0 | 20163 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0068 | 0/0 | 20166 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0069 | 0/0 | 20167 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0071 | 0/0 | 20159 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0072 | 0/0 | 20167 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0073 | 0/0 | 20165 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0074 | 0/0 | 20169 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0075 | 0/0 | 20170 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0076 | 0/0 | 20168 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0077 | 0/0 | 20172 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0078 | 0/0 | 20168 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0079 | 0/0 | 20166 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0080 | 0/0 | 20166 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0081 | 0/0 | 20166 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0082 | 0/0 | 20168 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0083 | 0/0 | 20164 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0084 | 0/0 | 20167 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0085 | 0/0 | 20166 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0130 | 0/0 | 20179 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0131 | 0/0 | 20177 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0132 | 0/0 | 20178 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0133 | 0/0 | 20177 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0134 | 0/0 | 20177 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0135 | 0/0 | 20178 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0136 | 0/0 | 20173 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0137 | 0/0 | 20174 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0005t0146 | 0/0 | 20166 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0044 | 0/0 | 20107 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0045 | 0/0 | 20156 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0046 | 0/0 | 20163 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0111 | 0/0 | 20156 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0140 | 0/0 | 20163 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0149 | 0/0 | 20168 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0151 | 0/0 | 20166 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0183 | 0/0 | 20157 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0184 | 0/0 | 20166 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0185 | 0/0 | 20106 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0186 | 0/0 | 20156 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0187 | 0/0 | 20156 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0188 | 0/0 | 20160 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0191 | 0/0 | 20399 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0006t0264 | 0/0 | 20179 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0004 | 0/0 | 20166 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0017 | 0/0 | 20163 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0037 | 0/0 | 20163 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0038 | 0/0 | 20164 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0152 | 0/0 | 20164 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0153 | 0/0 | 20165 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0154 | 0/0 | 20164 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0007t0156 | 0/0 | 20165 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0016 | 0/0 | 20177 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0021 | 0/0 | 20162 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0047 | 0/0 | 20115 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0128 | 0/0 | 20177 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0129 | 0/0 | 20178 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0189 | 0/0 | 20112 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0009t0190 | 0/0 | 20115 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0014t0059 | 0/0 | 20165 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0015t0267 | 0/0 | 20169 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0015t0268 | 0/0 | 20165 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0017t0028 | 0/0 | 20169 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0018t0214 | 0/0 | 20163 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0001c0024t0169 | 0/0 | 20166 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0003 | 0/0 | 20158 | 8 | 0 | 1 | 7 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0009 | 0/0 | 20158 | 4 | 0 | 2 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0013 | 0/0 | 20159 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0014 | 0/0 | 20157 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0015 | 0/0 | 20157 | 3 | 1 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0030 | 0/0 | 20156 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0031 | 0/0 | 20159 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0032 | 0/0 | 20158 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0033 | 0/0 | 20158 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0041 | 0/0 | 20115 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0042 | 0/0 | 20114 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0043 | 0/0 | 20157 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0066 | 0/0 | 20153 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0086 | 0/0 | 20157 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0087 | 0/0 | 20117 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0088 | 0/0 | 20110 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0089 | 0/0 | 20159 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0090 | 0/0 | 20158 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0091 | 0/0 | 20160 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0092 | 0/0 | 20160 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0093 | 0/0 | 20158 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0094 | 0/0 | 20159 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0095 | 0/0 | 20159 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0096 | 0/0 | 20109 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0097 | 0/0 | 20158 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0098 | 0/0 | 20157 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0099 | 0/0 | 20157 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0100 | 0/0 | 20158 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0102 | 0/0 | 20158 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0103 | 0/0 | 20157 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0104 | 0/0 | 20157 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0105 | 0/0 | 20157 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0107 | 0/0 | 20156 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0108 | 0/0 | 20158 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0109 | 0/0 | 20156 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0110 | 0/0 | 20157 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0173 | 0/0 | 20158 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0174 | 0/0 | 20156 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0176 | 0/0 | 20114 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0177 | 0/0 | 20114 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0178 | 0/0 | 20030 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0179 | 0/0 | 20029 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0002t0180 | 0/0 | 20172 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0012t0041 | 0/0 | 20115 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0012t0042 | 0/0 | 20114 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0012t0175 | 0/0 | 20115 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0019t0106 | 0/0 | 20157 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0021t0003 | 0/0 | 20158 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0002c0022t0101 | 0/0 | 18841 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0114 | 0/0 | 20169 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0192 | 0/0 | 20172 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0195 | 0/0 | 20170 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0196 | 0/0 | 20170 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0197 | 0/0 | 20267 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0199 | 0/0 | 20154 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0200 | 0/0 | 20170 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0206 | 0/0 | 20159 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0207 | 0/0 | 20160 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0208 | 0/0 | 20159 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0008t0209 | 0/0 | 18839 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0003c0016t0198 | 0/0 | 20161 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0004c0010t0010 | 0/0 | 20160 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0004c0010t0113 | 0/0 | 20161 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0004c0010t0117 | 0/0 | 20161 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0005c0011t0021 | 0/0 | 20162 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0005c0011t0022 | 0/0 | 20163 | 3 | 3 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006c0013t0143 | 0/0 | 20164 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006c0013t0144 | 0/0 | 20165 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006c0013t0167 | 0/0 | 20165 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0006c0020t0067 | 1/0 | 20166 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0007c0025t0035 | 0/0 | 20168 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
a0008c0023t0023 | 0/0 | 20120 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | copy fasta | chr3 | 133741393 | 133801641 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0005g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0006g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0011g0003 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0011g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0025g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0026g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0026g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0026g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0049g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0050g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0050g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0051g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0051g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0052g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0052g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0053g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0054g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0055g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0057g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0058g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0058g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0215g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0216g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0217g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0218g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0219g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0220g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0221g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0222g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0223g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0225g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0226g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0227g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0228g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0229g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0230g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0231g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0232g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0233g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0234g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0235g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0236g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0238g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0239g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0240g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0241g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0242g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0243g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0244g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0245g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0246g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0247g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0249g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0250g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0251g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0252g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0253g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0254g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0255g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0256g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0257g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0258g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0259g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0260g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0261g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0262g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0001t0263g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0007g0015 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0007g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0011g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0023g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0024g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0025g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0034g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0034g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0039g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0048g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0048g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0049g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0055g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0056g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0057g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0070g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0112g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0115g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0116g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0118g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0119g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0120g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0121g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0122g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0123g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0124g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0125g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0126g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0127g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0138g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0139g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0147g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0148g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0150g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0181g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0182g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0193g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0194g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0201g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0202g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0203g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0210g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0211g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0212g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0224g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0237g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0248g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0003t0265g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0008g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0018g0001 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0018g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0019g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0019g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0019g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0020g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0020g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0035g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0036g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0039g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0040g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0040g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0053g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0141g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0142g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0145g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0155g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0157g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0158g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0159g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0160g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0161g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0162g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0163g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0164g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0165g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0166g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0168g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0170g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0171g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0172g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0204g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0205g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0213g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0004t0266g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0016g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0027g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0027g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0028g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0029g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0029g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0060g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0061g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0062g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0063g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0064g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0065g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0068g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0069g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0071g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0072g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0073g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0074g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0075g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0076g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0077g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0078g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0079g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0080g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0081g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0082g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0083g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0084g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0085g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0130g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0131g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0132g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0133g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0134g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0135g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0136g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0137g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0005t0146g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0044g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0044g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0045g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0046g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0046g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0111g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0140g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0149g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0151g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0183g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0184g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0185g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0186g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0187g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0188g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0191g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0006t0264g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0017g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0017g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0017g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0037g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0037g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0038g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0038g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0152g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0153g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0154g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0007t0156g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0047g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0128g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0129g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0189g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0009t0190g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0014t0059g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0014t0059g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0015t0267g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0015t0268g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0017t0028g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0018t0214g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0001c0024t0169g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0003g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0009g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0013g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0013g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0014g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0014g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0015g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0030g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0030g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0031g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0031g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0032g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0032g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0033g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0041g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0042g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0043g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0043g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0066g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0086g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0087g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0088g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0089g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0090g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0091g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0092g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0093g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0094g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0095g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0096g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0097g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0098g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0099g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0100g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0102g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0103g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0104g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0105g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0107g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0108g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0109g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0110g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0173g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0174g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0176g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0177g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0178g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0179g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0002t0180g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0012t0041g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0012t0042g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0012t0175g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0019t0106g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0021t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0002c0022t0101g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0114g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0192g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0195g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0196g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0197g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0199g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0200g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0206g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0207g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0208g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0008t0209g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0003c0016t0198g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0004c0010t0010g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0004c0010t0113g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0004c0010t0117g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0005c0011t0021g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0005c0011t0022g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0005c0011t0022g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0006c0013t0143g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0006c0013t0144g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0006c0013t0167g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0006c0020t0067g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0007c0025t0035g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
a0008c0023t0023g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0034 | EUR | GBR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00099 | hp2 | a0001 | c0003 | t0119 | g0113 | EUR | GBR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00140 | hp1 | a0001 | c0004 | t0159 | g0192 | EUR | GBR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0020 | EUR | GBR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00280 | hp1 | a0001 | c0005 | t0081 | g0168 | EUR | FIN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00280 | hp2 | a0003 | c0008 | t0207 | g0026 | EUR | FIN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00323 | hp1 | a0001 | c0005 | t0072 | g0010 | EUR | FIN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00323 | hp2 | a0003 | c0008 | t0206 | g0026 | EUR | FIN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00423 | hp1 | a0001 | c0004 | t0172 | g0211 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00423 | hp2 | a0001 | c0003 | t0202 | g0222 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00544 | hp1 | a0002 | c0002 | t0013 | g0145 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00558 | hp2 | a0001 | c0004 | t0004 | g0001 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00609 | hp1 | a0002 | c0002 | t0032 | g0127 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00609 | hp2 | a0001 | c0003 | t0034 | g0114 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00621 | hp1 | a0001 | c0005 | t0077 | g0010 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00621 | hp2 | a0002 | c0002 | t0090 | g0138 | EAS | CHS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00639 | hp1 | a0001 | c0017 | t0028 | g0159 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00639 | hp2 | a0001 | c0005 | t0085 | g0147 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00642 | hp1 | a0001 | c0024 | t0169 | g0212 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00642 | hp2 | a0001 | c0003 | t0007 | g0043 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00733 | hp1 | a0003 | c0008 | t0199 | g0017 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00733 | hp2 | a0001 | c0003 | t0011 | g0047 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00735 | hp1 | a0003 | c0008 | t0192 | g0017 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00735 | hp2 | a0001 | c0003 | t0121 | g0111 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00738 | hp1 | a0003 | c0008 | t0195 | g0017 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00738 | hp2 | a0001 | c0005 | t0078 | g0010 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00741 | hp1 | a0001 | c0003 | t0049 | g0218 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG00741 | hp2 | a0001 | c0001 | t0215 | g0021 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01069 | hp1 | a0001 | c0005 | t0028 | g0165 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01069 | hp2 | a0002 | c0002 | t0109 | g0008 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01070 | hp1 | a0001 | c0004 | t0019 | g0045 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01070 | hp2 | a0006 | c0013 | t0167 | g0242 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01071 | hp1 | a0002 | c0002 | t0015 | g0008 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01071 | hp2 | a0001 | c0004 | t0168 | g0045 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01074 | hp1 | a0001 | c0005 | t0079 | g0010 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01074 | hp2 | a0006 | c0013 | t0143 | g0243 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01081 | hp1 | a0002 | c0002 | t0009 | g0004 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01081 | hp2 | a0001 | c0003 | t0203 | g0024 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01099 | hp1 | a0001 | c0004 | t0158 | g0194 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01099 | hp2 | a0001 | c0005 | t0075 | g0173 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01106 | hp1 | a0001 | c0003 | t0125 | g0157 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01106 | hp2 | a0003 | c0008 | t0196 | g0017 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01109 | hp1 | a0001 | c0003 | t0181 | g0025 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01109 | hp2 | a0001 | c0005 | t0064 | g0023 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01167 | hp1 | a0001 | c0001 | t0058 | g0244 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01167 | hp2 | a0001 | c0005 | t0083 | g0124 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01168 | hp1 | a0002 | c0002 | t0179 | g0040 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01168 | hp2 | a0001 | c0004 | t0018 | g0187 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01169 | hp1 | a0002 | c0002 | t0178 | g0040 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01169 | hp2 | a0001 | c0001 | t0058 | g0245 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01175 | hp1 | a0001 | c0004 | t0266 | g0191 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01175 | hp2 | a0001 | c0001 | t0216 | g0105 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01192 | hp1 | a0001 | c0003 | t0007 | g0043 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01192 | hp2 | a0001 | c0003 | t0055 | g0047 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01243 | hp1 | a0001 | c0005 | t0130 | g0009 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01243 | hp2 | a0001 | c0003 | t0148 | g0108 | AMR | PUR | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01255 | hp2 | a0001 | c0001 | t0254 | g0003 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01256 | hp1 | a0002 | c0002 | t0043 | g0004 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01256 | hp2 | a0001 | c0001 | t0219 | g0104 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01257 | hp1 | a0001 | c0001 | t0242 | g0099 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01257 | hp2 | a0001 | c0003 | t0048 | g0220 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01258 | hp1 | a0001 | c0003 | t0048 | g0024 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01258 | hp2 | a0002 | c0002 | t0043 | g0007 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01261 | hp1 | a0003 | c0008 | t0114 | g0172 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01261 | hp2 | a0001 | c0004 | t0035 | g0200 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01346 | hp2 | a0002 | c0002 | t0009 | g0004 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01358 | hp1 | a0001 | c0001 | t0223 | g0072 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01358 | hp2 | a0001 | c0003 | t0211 | g0024 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01361 | hp2 | a0001 | c0001 | t0233 | g0080 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01433 | hp1 | a0001 | c0001 | t0057 | g0102 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01433 | hp2 | a0001 | c0004 | t0040 | g0193 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01496 | hp1 | a0001 | c0005 | t0060 | g0160 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01496 | hp2 | a0001 | c0003 | t0056 | g0051 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01515 | hp1 | a0001 | c0001 | t0217 | g0021 | EUR | IBS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01515 | hp2 | a0001 | c0005 | t0076 | g0175 | EUR | IBS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01516 | hp1 | a0001 | c0003 | t0007 | g0176 | EUR | IBS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01516 | hp2 | a0001 | c0004 | t0018 | g0001 | EUR | IBS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01517 | hp1 | a0001 | c0004 | t0162 | g0001 | EUR | IBS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01517 | hp2 | a0001 | c0001 | t0218 | g0021 | EUR | IBS | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01884 | hp1 | a0002 | c0002 | t0030 | g0128 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01884 | hp2 | a0001 | c0005 | t0074 | g0174 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01891 | hp1 | a0001 | c0006 | t0264 | g0059 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01891 | hp2 | a0001 | c0005 | t0027 | g0163 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01928 | hp1 | a0001 | c0004 | t0020 | g0001 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01928 | hp2 | a0001 | c0003 | t0210 | g0011 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01943 | hp2 | a0001 | c0001 | t0055 | g0101 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01952 | hp1 | a0001 | c0003 | t0139 | g0219 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01952 | hp2 | a0006 | c0013 | t0144 | g0226 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01975 | hp1 | a0001 | c0001 | t0239 | g0091 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01975 | hp2 | a0001 | c0003 | t0024 | g0011 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01978 | hp1 | a0002 | c0002 | t0032 | g0140 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01978 | hp2 | a0001 | c0001 | t0240 | g0014 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01981 | hp2 | a0001 | c0003 | t0193 | g0224 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01993 | hp1 | a0001 | c0003 | t0024 | g0011 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01993 | hp2 | a0001 | c0001 | t0227 | g0002 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02015 | hp1 | a0001 | c0004 | t0004 | g0001 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02015 | hp2 | a0002 | c0002 | t0014 | g0130 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02027 | hp1 | a0007 | c0025 | t0035 | g0213 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02027 | hp2 | a0002 | c0002 | t0066 | g0131 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02040 | hp1 | a0001 | c0003 | t0039 | g0223 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02040 | hp2 | a0002 | c0002 | t0014 | g0150 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02055 | hp1 | a0001 | c0005 | t0063 | g0155 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02055 | hp2 | a0001 | c0001 | t0261 | g0068 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02056 | hp2 | a0002 | c0002 | t0031 | g0146 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02071 | hp1 | a0001 | c0005 | t0071 | g0010 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02080 | hp1 | a0001 | c0001 | t0258 | g0249 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02132 | hp1 | a0002 | c0002 | t0014 | g0132 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02132 | hp2 | a0001 | c0004 | t0004 | g0197 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02135 | hp1 | a0002 | c0022 | t0101 | g0143 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02135 | hp2 | a0001 | c0001 | t0221 | g0074 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02145 | hp1 | a0001 | c0006 | t0184 | g0029 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02145 | hp2 | a0001 | c0003 | t0115 | g0137 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02155 | hp1 | a0001 | c0004 | t0004 | g0195 | EAS | CDX | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02155 | hp2 | a0001 | c0001 | t0251 | g0002 | EAS | CDX | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CDX | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02165 | hp2 | a0001 | c0003 | t0201 | g0011 | EAS | CDX | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02257 | hp1 | a0001 | c0006 | t0183 | g0061 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02257 | hp2 | a0001 | c0003 | t0023 | g0025 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02280 | hp1 | a0001 | c0006 | t0044 | g0229 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02280 | hp2 | a0002 | c0002 | t0030 | g0008 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02300 | hp1 | a0001 | c0003 | t0024 | g0011 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02300 | hp2 | a0001 | c0001 | t0255 | g0033 | AMR | PEL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02451 | hp1 | a0001 | c0005 | t0016 | g0009 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02451 | hp2 | a0001 | c0005 | t0012 | g0023 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02523 | hp1 | a0001 | c0001 | t0238 | g0067 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02523 | hp2 | a0001 | c0001 | t0229 | g0005 | EAS | KHV | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02572 | hp1 | a0001 | c0003 | t0150 | g0097 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02572 | hp2 | a0001 | c0005 | t0069 | g0116 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02602 | hp1 | a0001 | c0004 | t0165 | g0001 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02602 | hp2 | a0001 | c0001 | t0236 | g0100 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02615 | hp1 | a0001 | c0003 | t0127 | g0152 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02615 | hp2 | a0001 | c0009 | t0016 | g0056 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02622 | hp1 | a0001 | c0005 | t0012 | g0153 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02622 | hp2 | a0001 | c0001 | t0252 | g0027 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02630 | hp1 | a0001 | c0003 | t0122 | g0171 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02630 | hp2 | a0008 | c0023 | t0023 | g0228 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02647 | hp1 | a0001 | c0005 | t0068 | g0095 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02647 | hp2 | a0001 | c0015 | t0267 | g0182 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02698 | hp1 | a0002 | c0012 | t0041 | g0070 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02698 | hp2 | a0001 | c0001 | t0011 | g0020 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02717 | hp1 | a0001 | c0005 | t0016 | g0037 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02717 | hp2 | a0001 | c0006 | t0046 | g0180 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02723 | hp1 | a0001 | c0005 | t0135 | g0009 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02723 | hp2 | a0001 | c0006 | t0046 | g0179 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02735 | hp2 | a0001 | c0004 | t0006 | g0206 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02738 | hp1 | a0001 | c0001 | t0256 | g0106 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02738 | hp2 | a0002 | c0002 | t0093 | g0133 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02809 | hp1 | a0001 | c0005 | t0131 | g0009 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02809 | hp2 | a0001 | c0003 | t0056 | g0051 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02818 | hp1 | a0001 | c0005 | t0065 | g0154 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02818 | hp2 | a0001 | c0009 | t0189 | g0013 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02886 | hp1 | a0001 | c0005 | t0132 | g0009 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02886 | hp2 | a0001 | c0006 | t0140 | g0178 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02895 | hp1 | a0001 | c0006 | t0044 | g0048 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02895 | hp2 | a0001 | c0018 | t0214 | g0177 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02896 | hp1 | a0001 | c0009 | t0128 | g0042 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02896 | hp2 | a0001 | c0014 | t0059 | g0238 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02897 | hp1 | a0001 | c0006 | t0185 | g0048 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02897 | hp2 | a0001 | c0009 | t0129 | g0042 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02922 | hp1 | a0001 | c0009 | t0021 | g0087 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02922 | hp2 | a0005 | c0011 | t0021 | g0018 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02965 | hp1 | a0005 | c0011 | t0021 | g0018 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02965 | hp2 | a0001 | c0006 | t0188 | g0029 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02970 | hp1 | a0001 | c0005 | t0073 | g0158 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02970 | hp2 | a0001 | c0005 | t0146 | g0055 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02976 | hp1 | a0005 | c0011 | t0022 | g0028 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02976 | hp2 | a0001 | c0003 | t0023 | g0025 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03017 | hp2 | a0001 | c0001 | t0263 | g0248 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03041 | hp1 | a0001 | c0005 | t0136 | g0094 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03041 | hp2 | a0005 | c0011 | t0022 | g0018 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03098 | hp1 | a0002 | c0002 | t0174 | g0184 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03098 | hp2 | a0001 | c0004 | t0205 | g0046 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03139 | hp1 | a0001 | c0005 | t0027 | g0023 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03139 | hp2 | a0001 | c0003 | t0182 | g0227 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03195 | hp1 | a0001 | c0006 | t0045 | g0030 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03195 | hp2 | a0001 | c0003 | t0147 | g0241 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03209 | hp1 | a0001 | c0003 | t0212 | g0239 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03209 | hp2 | a0001 | c0006 | t0186 | g0060 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03225 | hp1 | a0001 | c0014 | t0059 | g0237 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03225 | hp2 | a0001 | c0006 | t0191 | g0062 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03239 | hp1 | a0002 | c0019 | t0106 | g0135 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03239 | hp2 | a0001 | c0003 | t0007 | g0015 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03453 | hp1 | a0001 | c0005 | t0134 | g0037 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03453 | hp2 | a0005 | c0011 | t0022 | g0028 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03486 | hp1 | a0001 | c0001 | t0253 | g0027 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03486 | hp2 | a0001 | c0005 | t0062 | g0164 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03490 | hp1 | a0001 | c0001 | t0259 | g0082 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03490 | hp2 | a0001 | c0001 | t0054 | g0038 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03491 | hp1 | a0003 | c0008 | t0208 | g0090 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03491 | hp2 | a0001 | c0003 | t0124 | g0156 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03492 | hp1 | a0001 | c0003 | t0007 | g0015 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03492 | hp2 | a0001 | c0001 | t0054 | g0038 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03516 | hp1 | a0002 | c0002 | t0086 | g0041 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03516 | hp2 | a0001 | c0003 | t0112 | g0107 | AFR | ESN | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03540 | hp1 | a0001 | c0005 | t0012 | g0166 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03540 | hp2 | a0001 | c0001 | t0230 | g0034 | AFR | GWD | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03579 | hp1 | a0001 | c0009 | t0047 | g0013 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03579 | hp2 | a0002 | c0002 | t0108 | g0126 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03654 | hp1 | a0002 | c0002 | t0110 | g0008 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03654 | hp2 | a0003 | c0008 | t0197 | g0050 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03669 | hp1 | a0001 | c0004 | t0008 | g0016 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03669 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03688 | hp1 | a0002 | c0002 | t0041 | g0049 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03688 | hp2 | a0001 | c0004 | t0161 | g0001 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03704 | hp1 | a0001 | c0004 | t0142 | g0190 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03710 | hp1 | a0001 | c0003 | t0120 | g0112 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03710 | hp2 | a0003 | c0008 | t0209 | g0026 | SAS | PJL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03831 | hp1 | a0001 | c0001 | t0049 | g0103 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03831 | hp2 | a0003 | c0016 | t0198 | g0231 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03834 | hp1 | a0002 | c0012 | t0042 | g0071 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0016 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03942 | hp1 | a0002 | c0002 | t0107 | g0149 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04115 | hp1 | a0001 | c0001 | t0243 | g0052 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04115 | hp2 | a0002 | c0002 | t0094 | g0008 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04184 | hp1 | a0003 | c0008 | t0200 | g0050 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04184 | hp2 | a0002 | c0002 | t0095 | g0041 | SAS | BEB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04199 | hp1 | a0002 | c0012 | t0175 | g0053 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04199 | hp2 | a0001 | c0003 | t0034 | g0110 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04204 | hp1 | a0001 | c0007 | t0152 | g0250 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04204 | hp2 | a0001 | c0003 | t0126 | g0015 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG04228 | hp2 | a0001 | c0001 | t0249 | g0002 | SAS | STU | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18522 | hp1 | a0002 | c0002 | t0033 | g0039 | AFR | YRI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18522 | hp2 | a0001 | c0001 | t0262 | g0069 | AFR | YRI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18612 | hp2 | a0001 | c0005 | t0084 | g0010 | EAS | CHB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18906 | hp1 | a0001 | c0009 | t0190 | g0013 | AFR | YRI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18906 | hp2 | a0001 | c0003 | t0138 | g0125 | AFR | YRI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18940 | hp1 | a0001 | c0005 | t0082 | g0044 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18941 | hp2 | a0001 | c0004 | t0040 | g0209 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18942 | hp1 | a0002 | c0002 | t0098 | g0008 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18942 | hp2 | a0001 | c0004 | t0171 | g0189 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18943 | hp1 | a0001 | c0004 | t0053 | g0016 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18943 | hp2 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18949 | hp1 | a0002 | c0002 | t0013 | g0007 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18949 | hp2 | a0001 | c0004 | t0160 | g0198 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18950 | hp1 | a0001 | c0001 | t0260 | g0012 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18951 | hp1 | a0001 | c0007 | t0037 | g0035 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18951 | hp2 | a0002 | c0002 | t0088 | g0142 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18953 | hp1 | a0001 | c0007 | t0156 | g0019 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18954 | hp2 | a0001 | c0004 | t0019 | g0225 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18957 | hp1 | a0001 | c0001 | t0241 | g0014 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18957 | hp2 | a0001 | c0001 | t0225 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18959 | hp1 | a0002 | c0002 | t0180 | g0049 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18959 | hp2 | a0001 | c0003 | t0025 | g0221 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18960 | hp2 | a0001 | c0001 | t0026 | g0247 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18962 | hp1 | a0001 | c0001 | t0220 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18962 | hp2 | a0004 | c0010 | t0010 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18963 | hp1 | a0001 | c0004 | t0155 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18963 | hp2 | a0001 | c0007 | t0017 | g0035 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18966 | hp1 | a0001 | c0001 | t0228 | g0005 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18966 | hp2 | a0001 | c0004 | t0005 | g0016 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18967 | hp1 | a0002 | c0002 | t0102 | g0139 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18967 | hp2 | a0001 | c0001 | t0235 | g0003 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18968 | hp1 | a0001 | c0001 | t0246 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18968 | hp2 | a0002 | c0002 | t0096 | g0141 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18969 | hp1 | a0001 | c0007 | t0154 | g0063 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18969 | hp2 | a0001 | c0007 | t0004 | g0088 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18970 | hp1 | a0001 | c0004 | t0036 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18971 | hp1 | a0002 | c0002 | t0097 | g0007 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18972 | hp1 | a0001 | c0001 | t0051 | g0083 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18972 | hp2 | a0002 | c0002 | t0091 | g0007 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18973 | hp1 | a0001 | c0001 | t0025 | g0032 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18973 | hp2 | a0001 | c0007 | t0038 | g0019 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18974 | hp1 | a0001 | c0001 | t0050 | g0251 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18974 | hp2 | a0001 | c0001 | t0050 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18979 | hp1 | a0002 | c0021 | t0003 | g0022 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18979 | hp2 | a0001 | c0001 | t0051 | g0085 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18980 | hp1 | a0001 | c0004 | t0036 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18980 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18982 | hp2 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18983 | hp1 | a0001 | c0007 | t0017 | g0019 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18983 | hp2 | a0001 | c0004 | t0213 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18984 | hp1 | a0001 | c0007 | t0017 | g0036 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18984 | hp2 | a0001 | c0001 | t0250 | g0073 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18986 | hp1 | a0002 | c0002 | t0100 | g0129 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18986 | hp2 | a0001 | c0001 | t0025 | g0032 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18988 | hp1 | a0001 | c0001 | t0222 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18988 | hp2 | a0001 | c0003 | t0194 | g0011 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18990 | hp2 | a0001 | c0004 | t0039 | g0204 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18991 | hp1 | a0002 | c0002 | t0092 | g0122 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18991 | hp2 | a0001 | c0004 | t0008 | g0207 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18993 | hp1 | a0002 | c0002 | t0105 | g0120 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18993 | hp2 | a0002 | c0002 | t0042 | g0234 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18995 | hp2 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18998 | hp1 | a0001 | c0001 | t0257 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18999 | hp1 | a0002 | c0002 | t0013 | g0004 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18999 | hp2 | a0001 | c0004 | t0004 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19002 | hp2 | a0002 | c0002 | t0176 | g0233 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19003 | hp2 | a0001 | c0005 | t0029 | g0170 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19005 | hp1 | a0002 | c0002 | t0103 | g0119 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19005 | hp2 | a0001 | c0004 | t0164 | g0201 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19006 | hp1 | a0002 | c0002 | t0104 | g0118 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19006 | hp2 | a0001 | c0003 | t0248 | g0208 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19007 | hp1 | a0001 | c0004 | t0004 | g0199 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19007 | hp2 | a0001 | c0001 | t0052 | g0086 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19009 | hp2 | a0001 | c0004 | t0145 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19010 | hp2 | a0002 | c0002 | t0015 | g0117 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19011 | hp1 | a0001 | c0001 | t0244 | g0215 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19011 | hp2 | a0001 | c0004 | t0020 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19030 | hp1 | a0001 | c0003 | t0224 | g0217 | AFR | LWK | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19030 | hp2 | a0001 | c0003 | t0057 | g0109 | AFR | LWK | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19043 | hp1 | a0001 | c0001 | t0226 | g0033 | AFR | LWK | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19043 | hp2 | a0001 | c0003 | t0070 | g0121 | AFR | LWK | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19055 | hp1 | a0001 | c0007 | t0037 | g0036 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19055 | hp2 | a0001 | c0004 | t0020 | g0186 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19056 | hp1 | a0001 | c0005 | t0080 | g0162 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19056 | hp2 | a0001 | c0001 | t0026 | g0253 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19057 | hp1 | a0001 | c0004 | t0019 | g0205 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19057 | hp2 | a0001 | c0001 | t0026 | g0246 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19058 | hp1 | a0001 | c0004 | t0157 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19058 | hp2 | a0001 | c0001 | t0247 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19060 | hp1 | a0001 | c0004 | t0170 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19060 | hp2 | a0002 | c0002 | t0173 | g0236 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19062 | hp1 | a0001 | c0003 | t0118 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19062 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19064 | hp1 | a0001 | c0003 | t0010 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19065 | hp1 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19065 | hp2 | a0001 | c0004 | t0002 | g0214 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19066 | hp1 | a0004 | c0010 | t0010 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19066 | hp2 | a0001 | c0005 | t0029 | g0044 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19067 | hp1 | a0001 | c0001 | t0231 | g0210 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19067 | hp2 | a0004 | c0010 | t0117 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19074 | hp1 | a0001 | c0004 | t0004 | g0203 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19074 | hp2 | a0002 | c0002 | t0009 | g0004 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19075 | hp1 | a0004 | c0010 | t0010 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19075 | hp2 | a0001 | c0001 | t0245 | g0054 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19077 | hp2 | a0001 | c0004 | t0141 | g0001 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19078 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19078 | hp2 | a0002 | c0002 | t0031 | g0022 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19083 | hp1 | a0001 | c0001 | t0052 | g0076 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19083 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19087 | hp1 | a0002 | c0002 | t0089 | g0007 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19087 | hp2 | a0001 | c0004 | t0166 | g0196 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19088 | hp1 | a0001 | c0003 | t0123 | g0115 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19088 | hp2 | a0002 | c0002 | t0099 | g0134 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19090 | hp1 | a0001 | c0007 | t0038 | g0084 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19090 | hp2 | a0001 | c0004 | t0163 | g0181 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19091 | hp1 | a0004 | c0010 | t0113 | g0006 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19091 | hp2 | a0001 | c0004 | t0004 | g0188 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19240 | hp1 | a0001 | c0015 | t0268 | g0230 | AFR | YRI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA19240 | hp2 | a0001 | c0006 | t0187 | g0058 | AFR | YRI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20129 | hp1 | a0001 | c0005 | t0137 | g0096 | AFR | ASW | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20129 | hp2 | a0001 | c0004 | t0204 | g0046 | AFR | ASW | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20752 | hp1 | a0001 | c0001 | t0232 | g0098 | EUR | TSI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20752 | hp2 | a0001 | c0003 | t0007 | g0015 | EUR | TSI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20805 | hp1 | a0002 | c0002 | t0087 | g0169 | EUR | TSI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20805 | hp2 | a0001 | c0003 | t0116 | g0123 | EUR | TSI | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20905 | hp1 | a0001 | c0007 | t0153 | g0185 | SAS | GIH | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20905 | hp2 | a0001 | c0001 | t0234 | g0002 | SAS | GIH | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG01123 | hp2 | a0001 | c0006 | t0111 | g0151 | AMR | CLM | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02486 | hp1 | a0002 | c0002 | t0177 | g0235 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02486 | hp2 | a0001 | c0003 | t0265 | g0216 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02559 | hp1 | a0001 | c0006 | t0149 | g0089 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG02559 | hp2 | a0001 | c0006 | t0045 | g0030 | AFR | ACB | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03471 | hp1 | a0001 | c0005 | t0061 | g0161 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG03471 | hp2 | a0002 | c0002 | t0033 | g0039 | AFR | MSL | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG06807 | hp1 | a0001 | c0005 | t0133 | g0009 | AFR | USA | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
HG06807 | hp2 | a0001 | c0009 | t0047 | g0013 | AFR | USA | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18955 | hp1 | a0002 | c0002 | t0009 | g0148 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA18955 | hp2 | a0001 | c0001 | t0053 | g0002 | EAS | JPT | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20300 | hp1 | a0001 | c0006 | t0151 | g0057 | AFR | USA | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | USA | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA21309 | hp1 | a0001 | c0003 | t0237 | g0240 | AFR | LWK | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
NA21309 | hp2 | a0002 | c0002 | t0015 | g0008 | AFR | LWK | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0018 | g0001 | REF | REF | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
homoSapiens_grch38 | hp1 | a0006 | c0020 | t0067 | g0167 | REF | REF | TF_chr3_133741393_133801641 | TF | chr3 | 133741393 | 133801641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:133755381
|
C | T | 1 | a0007 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.521C>T | p.Ser174Leu | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/17 | 569/20166 | 521/2097 | 174/698 | chr3 | 133755381 | ||
chr3:133756968
|
G | A | 1 | a0003 | 12 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
missense_variant | MODERATE | c.829G>A | p.Gly277Ser | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/17 | 877/20166 | 829/2097 | 277/698 | chr3 | 133756968 | ||
chr3:133757785
|
A | G | 1 | a0005 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.887A>G | p.Asp296Gly | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/17 | 935/20166 | 887/2097 | 296/698 | chr3 | 133757785 | ||
chr3:133757875
|
C | G | 1 | a0008 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.977C>G | p.Pro326Arg | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/17 | 1025/20166 | 977/2097 | 326/698 | chr3 | 133757875 | ||
chr3:133757934
|
C | T | 1 | a0004 | 5 | NA18962.hp2 NA19066.hp1 NA19067.hp2 others(2): Show |
missense_variant | MODERATE | c.1036C>T | p.Arg346Trp | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/17 | 1084/20166 | 1036/2097 | 346/698 | chr3 | 133757934 | ||
chr3:133766289
|
A | G | 7 | a0001a0002a0003others(4): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
missense_variant | MODERATE | c.1342A>G | p.Ile448Val | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/17 | 1390/20166 | 1342/2097 | 448/698 | chr3 | 133766289 | ||
chr3:133775510
|
C | T | 1 | a0002 | 70 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
missense_variant | MODERATE | c.1765C>T | p.Pro589Ser | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/17 | 1813/20166 | 1765/2097 | 589/698 | chr3 | 133775510 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:133748563
|
T | C | 1 | a0003c0016 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.195T>C | p.Leu65Leu | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/17 | 243/20166 | 195/2097 | 65/698 | chr3 | 133748563 | ||
chr3:133754502
|
G | A | 1 | a0001c0017 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.333G>A | p.Gln111Gln | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/17 | 381/20166 | 333/2097 | 111/698 | chr3 | 133754502 | ||
chr3:133754601
|
C | T | 1 | a0005c0011 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.432C>T | p.Ser144Ser | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/17 | 480/20166 | 432/2097 | 144/698 | chr3 | 133754601 | ||
chr3:133755442
|
A | G | 1 | a0005c0011 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.582A>G | p.Pro194Pro | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/17 | 630/20166 | 582/2097 | 194/698 | chr3 | 133755442 | ||
chr3:133755484
|
G | A | 3 | a0001c0001a0001c0007a0002c0012 | 122 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(119): Show |
synonymous_variant | LOW | c.624G>A | p.Ser208Ser | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/17 | 672/20166 | 624/2097 | 208/698 | chr3 | 133755484 | ||
chr3:133756878
|
C | T | 6 | a0001c0004a0001c0024a0003c0008others(3): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
synonymous_variant | LOW | c.739C>T | p.Leu247Leu | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/17 | 787/20166 | 739/2097 | 247/698 | chr3 | 133756878 | ||
chr3:133756943
|
T | C | 3 | a0001c0006a0001c0009a0001c0018 | 27 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(24): Show |
synonymous_variant | LOW | c.804T>C | p.His268His | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/17 | 852/20166 | 804/2097 | 268/698 | chr3 | 133756943 | ||
chr3:133756949
|
C | T | 1 | a0001c0018 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.810C>T | p.Val270Val | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/17 | 858/20166 | 810/2097 | 270/698 | chr3 | 133756949 | ||
chr3:133757891
|
G | A | 1 | a0001c0014 | 2 | HG02896.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.993G>A | p.Lys331Lys | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/17 | 1041/20166 | 993/2097 | 331/698 | chr3 | 133757891 | ||
chr3:133759221
|
G | A | 1 | a0002c0019 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1095G>A | p.Ala365Ala | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/17 | 1143/20166 | 1095/2097 | 365/698 | chr3 | 133759221 | ||
chr3:133766423
|
C | T | 1 | a0002c0022 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.1476C>T | p.His492His | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/17 | 1524/20166 | 1476/2097 | 492/698 | chr3 | 133766423 | ||
chr3:133768114
|
G | C | 8 | a0001c0005a0001c0007a0001c0009others(5): Show | 69 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(66): Show |
synonymous_variant | LOW | c.1572G>C | p.Leu524Leu | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/17 | 1620/20166 | 1572/2097 | 524/698 | chr3 | 133768114 | ||
chr3:133768144
|
C | T | 2 | a0001c0014a0001c0015 | 4 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.1602C>T | p.Tyr534Tyr | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/17 | 1650/20166 | 1602/2097 | 534/698 | chr3 | 133768144 | ||
chr3:133768156
|
C | T | 1 | a0005c0011 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.1614C>T | p.Gly538Gly | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/17 | 1662/20166 | 1614/2097 | 538/698 | chr3 | 133768156 | ||
chr3:133775551
|
G | A | 1 | a0002c0021 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1806G>A | p.Pro602Pro | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/17 | 1854/20166 | 1806/2097 | 602/698 | chr3 | 133775551 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:133746439
|
A | G | 190 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(187): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
5_prime_UTR_variant | MODIFIER | c.-2A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/17 | 2 | chr3 | 133746439 | |||||
chr3:133779030
|
G | A | 8 | a0001c0005t0012a0001c0005t0027a0001c0005t0060others(5): Show | 11 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*410G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 410 | chr3 | 133779030 | |||||
chr3:133779035
|
C | T | 4 | a0001c0003t0138a0001c0014t0059a0001c0015t0267others(1): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*415C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 415 | chr3 | 133779035 | |||||
chr3:133779236
|
A | G | 1 | a0001c0004t0266 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*616A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 616 | chr3 | 133779236 | |||||
chr3:133779355
|
T | G | 1 | a0001c0005t0060 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*735T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 735 | chr3 | 133779355 | |||||
chr3:133779884
|
TG | T | 4 | a0001c0003t0138a0001c0014t0059a0001c0015t0267others(1): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1265delG | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1265 | chr3 | 133779884 | |||||
chr3:133779897
|
A | G | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(96): Show | 152 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1277A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1277 | chr3 | 133779897 | |||||
chr3:133779945
|
G | A | 94 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(91): Show | 146 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1325G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1325 | chr3 | 133779945 | |||||
chr3:133780179
|
C | T | 1 | a0001c0018t0214 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1559C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1559 | chr3 | 133780179 | |||||
chr3:133780218
|
C | T | 3 | a0001c0001t0049a0001c0003t0049a0001c0003t0121 | 3 | HG00735.hp2 HG00741.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1598C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1598 | chr3 | 133780218 | |||||
chr3:133780219
|
G | A | 86 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(83): Show | 138 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1599G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1599 | chr3 | 133780219 | |||||
chr3:133780315
|
G | A | 1 | a0001c0003t0139 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1695G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 1695 | chr3 | 133780315 | |||||
chr3:133780820
|
C | T | 1 | a0001c0003t0265 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2200C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2200 | chr3 | 133780820 | |||||
chr3:133781094
|
G | A | 5 | a0001c0001t0215a0001c0001t0216a0001c0001t0217others(2): Show | 5 | HG00741.hp2 HG01175.hp2 HG01256.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2474G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2474 | chr3 | 133781094 | |||||
chr3:133781229
|
T | C | 1 | a0001c0006t0140 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2609T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2609 | chr3 | 133781229 | |||||
chr3:133781270
|
C | T | 1 | a0001c0004t0213 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2650 | chr3 | 133781270 | |||||
chr3:133781287
|
G | C | 1 | a0001c0001t0220 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2667 | chr3 | 133781287 | |||||
chr3:133781450
|
A | G | 40 | a0001c0001t0025a0001c0001t0049a0001c0003t0010others(37): Show | 47 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2830A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2830 | chr3 | 133781450 | |||||
chr3:133781518
|
C | G | 5 | a0001c0003t0112a0001c0006t0191a0001c0009t0047others(2): Show | 6 | HG02818.hp2 HG03225.hp2 HG03516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2898C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2898 | chr3 | 133781518 | |||||
chr3:133781580
|
G | T | 11 | a0001c0006t0044a0001c0006t0045a0001c0006t0046others(8): Show | 14 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2960G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 2960 | chr3 | 133781580 | |||||
chr3:133781906
|
A | G | 1 | a0001c0001t0263 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3286A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3286 | chr3 | 133781906 | |||||
chr3:133781933
|
A | T | 5 | a0001c0003t0112a0001c0006t0191a0001c0009t0047others(2): Show | 6 | HG02818.hp2 HG03225.hp2 HG03516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3313A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3313 | chr3 | 133781933 | |||||
chr3:133782274
|
A | G | 1 | a0001c0003t0182 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3654A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3654 | chr3 | 133782274 | |||||
chr3:133782358
|
T | C | 1 | a0002c0002t0066 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3738T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3738 | chr3 | 133782358 | |||||
chr3:133782422
|
T | TAC | 72 | a0001c0001t0058a0001c0001t0261a0001c0001t0262others(69): Show | 99 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*3820_*3821dupCA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3822 | INFO_REALIGN_3_PRIME | chr3 | 133782422 | ||||
chr3:133782422
|
T | TACAC | 14 | a0001c0003t0112a0001c0005t0016a0001c0005t0130others(11): Show | 15 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3818_*3821dupCACA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3822 | INFO_REALIGN_3_PRIME | chr3 | 133782422 | ||||
chr3:133782505
|
A | G | 4 | a0001c0003t0138a0001c0014t0059a0001c0015t0267others(1): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3885A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3885 | chr3 | 133782505 | |||||
chr3:133782533
|
A | T | 1 | a0001c0003t0265 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3913 | chr3 | 133782533 | |||||
chr3:133782547
|
T | C | 2 | a0002c0002t0030a0002c0002t0086 | 3 | HG01884.hp1 HG02280.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3927T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3927 | chr3 | 133782547 | |||||
chr3:133782552
|
G | A | 9 | a0001c0006t0044a0001c0006t0045a0001c0006t0111others(6): Show | 11 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3932G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3932 | chr3 | 133782552 | |||||
chr3:133782563
|
C | T | 104 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(101): Show | 161 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*3943C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 3943 | chr3 | 133782563 | |||||
chr3:133782633
|
G | A | 13 | a0001c0005t0016a0001c0005t0130a0001c0005t0131others(10): Show | 14 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4013G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4013 | chr3 | 133782633 | |||||
chr3:133782685
|
G | A | 40 | a0001c0001t0025a0001c0001t0049a0001c0003t0010others(37): Show | 47 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4065G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4065 | chr3 | 133782685 | |||||
chr3:133782792
|
CA | C | 121 | a0001c0001t0025a0001c0001t0049a0001c0001t0050others(118): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*4189delA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4189 | INFO_REALIGN_3_PRIME | chr3 | 133782792 | ||||
chr3:133782792
|
CAA | C | 139 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(136): Show | 215 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*4188_*4189delAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4188 | INFO_REALIGN_3_PRIME | chr3 | 133782792 | ||||
chr3:133782809
|
AC | A | 9 | a0001c0006t0044a0001c0006t0045a0001c0006t0046others(6): Show | 12 | HG01123.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4190delC | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4190 | chr3 | 133782809 | |||||
chr3:133782810
|
C | A | 2 | a0001c0006t0183a0001c0006t0184 | 2 | HG02145.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4190C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4190 | chr3 | 133782810 | |||||
chr3:133782819
|
C | A | 6 | a0001c0001t0226a0001c0003t0147a0001c0003t0182others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4199C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4199 | chr3 | 133782819 | |||||
chr3:133782872
|
C | A | 3 | a0001c0001t0026a0001c0001t0050a0001c0003t0123 | 6 | NA18960.hp2 NA18974.hp1 NA18974.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4252C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4252 | chr3 | 133782872 | |||||
chr3:133782874
|
A | C | 49 | a0001c0003t0112a0001c0003t0138a0001c0006t0044others(46): Show | 60 | HG00609.hp1 HG01069.hp2 HG01071.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4254A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4254 | chr3 | 133782874 | |||||
chr3:133782925
|
G | A | 1 | a0001c0001t0227 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4305G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4305 | chr3 | 133782925 | |||||
chr3:133783307
|
G | T | 1 | a0001c0005t0065 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4687G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4687 | chr3 | 133783307 | |||||
chr3:133783361
|
T | C | 1 | a0001c0003t0122 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4741T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 4741 | chr3 | 133783361 | |||||
chr3:133783818
|
A | G | 1 | a0001c0001t0260 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5198A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5198 | chr3 | 133783818 | |||||
chr3:133783924
|
C | T | 1 | a0001c0003t0126 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5304C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5304 | chr3 | 133783924 | |||||
chr3:133783984
|
G | C | 2 | a0001c0004t0036a0001c0004t0141 | 3 | NA18970.hp1 NA18980.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5364G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5364 | chr3 | 133783984 | |||||
chr3:133784275
|
G | A | 7 | a0001c0003t0138a0001c0009t0021a0001c0014t0059others(4): Show | 11 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5655G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5655 | chr3 | 133784275 | |||||
chr3:133784466
|
T | TA | 25 | a0001c0001t0005a0001c0001t0011a0001c0001t0026others(22): Show | 36 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5853dupA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | INFO_REALIGN_3_PRIME | chr3 | 133784466 | ||||
chr3:133784466
|
T | TAA | 11 | a0001c0005t0016a0001c0005t0130a0001c0005t0131others(8): Show | 12 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5852_*5853dupAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | INFO_REALIGN_3_PRIME | chr3 | 133784466 | ||||
chr3:133784468
|
A | AAAT | 8 | a0001c0005t0028a0001c0005t0074a0001c0005t0075others(5): Show | 8 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5850_*5851insTAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5851 | INFO_REALIGN_3_PRIME | chr3 | 133784468 | ||||
chr3:133784471
|
A | AAAT | 4 | a0001c0003t0138a0001c0004t0157a0001c0004t0213others(1): Show | 4 | HG02647.hp2 NA18906.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5886_*5888dupATA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5889 | INFO_REALIGN_3_PRIME | chr3 | 133784471 | ||||
chr3:133784471
|
A | T | 20 | a0001c0004t0145a0001c0005t0028a0001c0005t0029others(17): Show | 22 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5851A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5851 | chr3 | 133784471 | |||||
chr3:133784471
|
AAAT | A | 32 | a0001c0001t0249a0001c0003t0147a0001c0003t0182others(29): Show | 39 | HG01074.hp2 HG01109.hp2 HG01169.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5886_*5888delATA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5886 | INFO_REALIGN_3_PRIME | chr3 | 133784471 | ||||
chr3:133784472
|
AAT | A | 29 | a0001c0003t0127a0002c0002t0003a0002c0002t0009others(26): Show | 48 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5854_*5855delTA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | INFO_REALIGN_3_PRIME | chr3 | 133784472 | ||||
chr3:133784472
|
AATAAT | A | 12 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(9): Show | 15 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5854_*5858delTAAT others(1): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | INFO_REALIGN_3_PRIME | chr3 | 133784472 | ||||
chr3:133784473
|
AT | A | 66 | a0001c0001t0025a0001c0001t0049a0001c0001t0223others(63): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5854delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | chr3 | 133784473 | |||||
chr3:133784473
|
ATAAT | A | 10 | a0001c0003t0120a0002c0002t0041a0002c0002t0042others(7): Show | 10 | HG01168.hp1 HG02486.hp1 HG02698.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5854_*5857delTAAT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | chr3 | 133784473 | |||||
chr3:133784473
|
ATAATAAT | A | 2 | a0001c0006t0046a0001c0006t0140 | 3 | HG02717.hp2 HG02723.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5854_*5860delTAAT others(3): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | chr3 | 133784473 | |||||
chr3:133784474
|
T | A | 82 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(79): Show | 135 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*5854T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5854 | chr3 | 133784474 | |||||
chr3:133784477
|
T | A | 191 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(188): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*5857T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5857 | chr3 | 133784477 | |||||
chr3:133784480
|
T | A | 176 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(173): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*5860T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5860 | chr3 | 133784480 | |||||
chr3:133784482
|
A | T | 4 | a0001c0001t0226a0001c0001t0252a0001c0001t0253others(1): Show | 5 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5862A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5862 | chr3 | 133784482 | |||||
chr3:133784483
|
T | A | 110 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(107): Show | 156 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*5863T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5863 | chr3 | 133784483 | |||||
chr3:133784486
|
T | A | 41 | a0001c0001t0221a0001c0001t0223a0001c0001t0228others(38): Show | 46 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*5866T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5866 | chr3 | 133784486 | |||||
chr3:133784489
|
T | A | 9 | a0001c0001t0228a0001c0001t0229a0001c0003t0023others(6): Show | 11 | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5869T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5869 | chr3 | 133784489 | |||||
chr3:133784567
|
A | G | 3 | a0001c0001t0252a0001c0001t0253a0001c0003t0056 | 4 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5947A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 5947 | chr3 | 133784567 | |||||
chr3:133784742
|
G | A | 1 | a0001c0001t0244 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6122G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6122 | chr3 | 133784742 | |||||
chr3:133784805
|
G | C | 7 | a0001c0003t0138a0001c0009t0021a0001c0014t0059others(4): Show | 11 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6185G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6185 | chr3 | 133784805 | |||||
chr3:133784883
|
C | A | 1 | a0001c0001t0257 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6263C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6263 | chr3 | 133784883 | |||||
chr3:133784906
|
C | T | 2 | a0001c0006t0046a0001c0006t0140 | 3 | HG02717.hp2 HG02723.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6286C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6286 | chr3 | 133784906 | |||||
chr3:133784922
|
TAACAATA others(1309): Show |
T | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(74): Show | 129 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*6319_*7634del | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6319 | INFO_REALIGN_3_PRIME | chr3 | 133784922 | ||||
chr3:133784938
|
TAGGGAGG others(42): Show |
T | 1 | a0001c0004t0158 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6347_*6395delTGGC others(45): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6347 | INFO_REALIGN_3_PRIME | chr3 | 133784938 | ||||
chr3:133785001
|
G | T | 1 | a0001c0005t0085 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6381G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6381 | chr3 | 133785001 | |||||
chr3:133785098
|
C | T | 8 | a0001c0003t0115a0001c0003t0116a0003c0008t0114others(5): Show | 8 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6478C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6478 | chr3 | 133785098 | |||||
chr3:133785137
|
CCCGCCCG others(42): Show |
C | 3 | a0001c0003t0023a0001c0003t0181a0008c0023t0023 | 4 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6536_*6584delTGTC others(45): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6536 | INFO_REALIGN_3_PRIME | chr3 | 133785137 | ||||
chr3:133785139
|
CGCCCGGC others(120): Show |
C | 2 | a0002c0002t0178a0002c0002t0179 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6536_*6662del | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6536 | INFO_REALIGN_3_PRIME | chr3 | 133785139 | ||||
chr3:133785143
|
C | T | 1 | a0002c0002t0093 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6523C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6523 | chr3 | 133785143 | |||||
chr3:133785160
|
C | T | 1 | a0002c0002t0173 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6540C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6540 | chr3 | 133785160 | |||||
chr3:133785189
|
G | A | 3 | a0001c0009t0047a0001c0009t0189a0001c0009t0190 | 4 | HG02818.hp2 HG03579.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6569G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6569 | chr3 | 133785189 | |||||
chr3:133785234
|
G | A | 2 | a0001c0005t0072a0001c0005t0079 | 2 | HG00323.hp1 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6614G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6614 | chr3 | 133785234 | |||||
chr3:133785238
|
G | A | 1 | a0001c0015t0268 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6618G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6618 | chr3 | 133785238 | |||||
chr3:133785260
|
C | T | 1 | a0001c0001t0226 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6640C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6640 | chr3 | 133785260 | |||||
chr3:133785272
|
GCCAGCCG others(42): Show |
G | 2 | a0002c0002t0088a0002c0002t0096 | 2 | NA18951.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6664_*6712delGTCC others(45): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6664 | INFO_REALIGN_3_PRIME | chr3 | 133785272 | ||||
chr3:133785279
|
GCCCCGTC others(43): Show |
G | 3 | a0001c0009t0047a0001c0009t0189a0001c0009t0190 | 4 | HG02818.hp2 HG03579.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6663_*6712delCGTC others(46): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6663 | INFO_REALIGN_3_PRIME | chr3 | 133785279 | ||||
chr3:133785284
|
G | A | 2 | a0002c0002t0178a0002c0002t0179 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6664G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6664 | chr3 | 133785284 | |||||
chr3:133785284
|
GTCCGGGA others(42): Show |
G | 2 | a0001c0006t0044a0001c0006t0185 | 3 | HG02280.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6688_*6736delGGCC others(45): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6688 | INFO_REALIGN_3_PRIME | chr3 | 133785284 | ||||
chr3:133785300
|
GGGGGGTC others(316): Show |
G | 3 | a0001c0001t0049a0001c0003t0049a0001c0003t0121 | 3 | HG00735.hp2 HG00741.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6686_*7008del | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6686 | INFO_REALIGN_3_PRIME | chr3 | 133785300 | ||||
chr3:133785308
|
G | A | 2 | a0002c0002t0178a0002c0002t0179 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6688G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6688 | chr3 | 133785308 | |||||
chr3:133785327
|
C | T | 16 | a0001c0001t0261a0001c0001t0262a0001c0003t0010others(13): Show | 19 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6707C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6707 | chr3 | 133785327 | |||||
chr3:133785333
|
A | G | 3 | a0001c0009t0047a0001c0009t0189a0001c0009t0190 | 4 | HG02818.hp2 HG03579.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6713A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6713 | chr3 | 133785333 | |||||
chr3:133785353
|
GGTCAGCC others(42): Show |
G | 1 | a0001c0004t0159 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6743_*6791delCCGC others(45): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6743 | INFO_REALIGN_3_PRIME | chr3 | 133785353 | ||||
chr3:133785377
|
G | A | 8 | a0001c0005t0012a0001c0005t0027a0001c0005t0060others(5): Show | 11 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6757G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6757 | chr3 | 133785377 | |||||
chr3:133785381
|
T | C | 13 | a0001c0001t0025a0001c0003t0024a0001c0003t0025others(10): Show | 17 | HG00423.hp2 HG01081.hp2 HG01257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6761T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6761 | chr3 | 133785381 | |||||
chr3:133785381
|
TGTCCGGG others(42): Show |
T | 8 | a0002c0002t0041a0002c0002t0042a0002c0002t0087others(5): Show | 8 | HG02486.hp1 HG02698.hp1 HG03688.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6782_*6830delTGTC others(45): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6782 | INFO_REALIGN_3_PRIME | chr3 | 133785381 | ||||
chr3:133785382
|
G | GTCCGGGA others(91): Show |
12 | a0001c0001t0025a0001c0003t0024a0001c0003t0025others(9): Show | 16 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6781_*6782insGGTC others(94): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6782 | INFO_REALIGN_3_PRIME | chr3 | 133785382 | ||||
chr3:133785382
|
G | GTCCGGGA others(189): Show |
1 | a0001c0003t0203 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6781_*6782insGGTC others(192): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6782 | INFO_REALIGN_3_PRIME | chr3 | 133785382 | ||||
chr3:133785490
|
G | T | 1 | a0002c0002t0173 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6870G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6870 | chr3 | 133785490 | |||||
chr3:133785494
|
T | TGGGGGGG others(222): Show |
1 | a0001c0006t0191 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6882_*6883insGTCA others(225): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6883 | INFO_REALIGN_3_PRIME | chr3 | 133785494 | ||||
chr3:133785604
|
G | GC | 209 | a0001c0001t0025a0001c0001t0226a0001c0001t0249others(206): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*6987dupC | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6988 | INFO_REALIGN_3_PRIME | chr3 | 133785604 | ||||
chr3:133785608
|
G | A | 1 | a0002c0002t0097 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6988G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 6988 | chr3 | 133785608 | |||||
chr3:133785619
|
A | AG | 182 | a0001c0001t0025a0001c0001t0226a0001c0001t0249others(179): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*7000dupG | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7001 | INFO_REALIGN_3_PRIME | chr3 | 133785619 | ||||
chr3:133785620
|
G | GGT | 25 | a0001c0004t0158a0001c0005t0074a0001c0005t0075others(22): Show | 41 | HG00544.hp1 HG00621.hp2 HG01081.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*7000_*7001insGT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7001 | chr3 | 133785620 | |||||
chr3:133785621
|
A | G | 27 | a0001c0004t0158a0001c0005t0071a0001c0005t0074others(24): Show | 43 | HG00544.hp1 HG00621.hp2 HG01081.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*7001A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7001 | chr3 | 133785621 | |||||
chr3:133785621
|
A | T | 182 | a0001c0001t0025a0001c0001t0226a0001c0001t0249others(179): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*7001A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7001 | chr3 | 133785621 | |||||
chr3:133785623
|
T | G | 209 | a0001c0001t0025a0001c0001t0226a0001c0001t0249others(206): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*7003T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7003 | chr3 | 133785623 | |||||
chr3:133785633
|
GC | G | 210 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(207): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*7022delC | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7022 | INFO_REALIGN_3_PRIME | chr3 | 133785633 | ||||
chr3:133785636
|
C | T | 5 | a0001c0003t0070a0001c0003t0148a0001c0003t0150others(2): Show | 5 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7016C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7016 | chr3 | 133785636 | |||||
chr3:133785657
|
C | T | 2 | a0001c0006t0046a0001c0006t0140 | 3 | HG02717.hp2 HG02723.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7037C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7037 | chr3 | 133785657 | |||||
chr3:133785733
|
C | A | 5 | a0001c0003t0070a0001c0003t0148a0001c0003t0150others(2): Show | 5 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7113C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7113 | chr3 | 133785733 | |||||
chr3:133785815
|
T | C | 101 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(98): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*7195T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7195 | chr3 | 133785815 | |||||
chr3:133785953
|
C | A | 1 | a0001c0004t0204 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7333C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7333 | chr3 | 133785953 | |||||
chr3:133786069
|
A | G | 7 | a0001c0003t0138a0001c0009t0021a0001c0014t0059others(4): Show | 11 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7449A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7449 | chr3 | 133786069 | |||||
chr3:133786075
|
C | T | 7 | a0001c0003t0138a0001c0009t0021a0001c0014t0059others(4): Show | 11 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7455C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7455 | chr3 | 133786075 | |||||
chr3:133786144
|
C | T | 1 | a0001c0005t0084 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7524C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7524 | chr3 | 133786144 | |||||
chr3:133786222
|
T | TA | 44 | a0001c0001t0260a0001c0003t0039a0001c0004t0004others(41): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*7620dupA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
T | TAA | 15 | a0001c0003t0024a0001c0003t0139a0001c0003t0193others(12): Show | 18 | HG01928.hp2 HG01952.hp1 HG01975.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*7619_*7620dupAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
T | TAAA | 12 | a0001c0003t0070a0001c0003t0147a0001c0003t0150others(9): Show | 12 | HG02572.hp1 HG02572.hp2 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7618_*7620dupAAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
T | TAAAA | 15 | a0001c0003t0118a0001c0003t0148a0001c0006t0044others(12): Show | 18 | HG01123.hp2 HG01243.hp2 HG02145.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*7617_*7620dupAAAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
T | TAAAAA | 4 | a0001c0003t0010a0001c0003t0112a0004c0010t0010others(1): Show | 6 | HG03516.hp2 NA18962.hp2 NA19064.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7616_*7620dupAAAA others(1): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
T | TAAAAAA | 10 | a0001c0003t0023a0001c0003t0181a0001c0005t0132others(7): Show | 13 | HG00609.hp1 HG01109.hp1 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7615_*7620dupAAAA others(2): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
T | TTA | 11 | a0001c0001t0025a0001c0001t0049a0001c0003t0025others(8): Show | 13 | HG00423.hp2 HG00735.hp2 HG00741.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7602_*7603insTA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7603 | chr3 | 133786222 | |||||
chr3:133786222
|
T | TTAAA | 10 | a0002c0002t0014a0002c0002t0090a0002c0002t0095others(7): Show | 12 | HG00621.hp2 HG01069.hp2 HG01106.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7602_*7603insTAAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7603 | chr3 | 133786222 | |||||
chr3:133786222
|
T | TTAAAA | 44 | a0001c0001t0249a0001c0003t0034a0001c0003t0115others(41): Show | 62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*7602_*7603insTAAA others(1): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7603 | chr3 | 133786222 | |||||
chr3:133786222
|
T | TTAAAAA | 12 | a0001c0001t0262a0001c0005t0016a0001c0005t0130others(9): Show | 13 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7602_*7603insTAAA others(2): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7603 | chr3 | 133786222 | |||||
chr3:133786222
|
TA | T | 6 | a0001c0003t0138a0001c0005t0061a0001c0005t0062others(3): Show | 7 | HG01109.hp2 HG02647.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7620delA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7620 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786222
|
TAA | T | 3 | a0001c0009t0021a0005c0011t0021a0005c0011t0022 | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7619_*7620delAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7619 | INFO_REALIGN_3_PRIME | chr3 | 133786222 | ||||
chr3:133786240
|
AC | A | 4 | a0001c0001t0252a0001c0003t0056a0001c0004t0036others(1): Show | 6 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7621delC | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | chr3 | 133786240 | |||||
chr3:133786241
|
C | A | 4 | a0001c0005t0071a0002c0002t0014a0002c0002t0066others(1): Show | 6 | HG00621.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7621C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7621 | chr3 | 133786241 | |||||
chr3:133786466
|
A | G | 4 | a0001c0001t0226a0001c0001t0252a0001c0001t0253others(1): Show | 5 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7846A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 7846 | chr3 | 133786466 | |||||
chr3:133786910
|
T | C | 4 | a0001c0001t0226a0001c0001t0252a0001c0001t0253others(1): Show | 5 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8290T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8290 | chr3 | 133786910 | |||||
chr3:133787042
|
C | T | 6 | a0001c0005t0012a0001c0005t0027a0001c0005t0060others(3): Show | 9 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8422C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8422 | chr3 | 133787042 | |||||
chr3:133787085
|
G | A | 1 | a0001c0001t0258 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8465G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8465 | chr3 | 133787085 | |||||
chr3:133787126
|
A | G | 3 | a0001c0009t0021a0005c0011t0021a0005c0011t0022 | 6 | HG02922.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8506A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8506 | chr3 | 133787126 | |||||
chr3:133787283
|
A | G | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(74): Show | 129 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*8663A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8663 | chr3 | 133787283 | |||||
chr3:133787373
|
G | A | 1 | a0001c0015t0268 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8753G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8753 | chr3 | 133787373 | |||||
chr3:133787420
|
G | A | 1 | a0001c0003t0122 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8800G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8800 | chr3 | 133787420 | |||||
chr3:133787463
|
A | G | 1 | a0001c0003t0122 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8843A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 8843 | chr3 | 133787463 | |||||
chr3:133787885
|
T | G | 15 | a0001c0001t0261a0001c0001t0262a0001c0003t0010others(12): Show | 18 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*9265T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9265 | chr3 | 133787885 | |||||
chr3:133787894
|
G | A | 20 | a0001c0001t0261a0001c0001t0262a0001c0003t0010others(17): Show | 23 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*9274G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9274 | chr3 | 133787894 | |||||
chr3:133787898
|
A | G | 1 | a0001c0004t0165 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9278A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9278 | chr3 | 133787898 | |||||
chr3:133788189
|
A | G | 6 | a0001c0005t0012a0001c0005t0027a0001c0005t0060others(3): Show | 9 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9569A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9569 | chr3 | 133788189 | |||||
chr3:133788218
|
G | C | 17 | a0001c0001t0025a0001c0001t0049a0001c0003t0024others(14): Show | 21 | HG00423.hp2 HG00735.hp2 HG00741.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*9598G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9598 | chr3 | 133788218 | |||||
chr3:133788253
|
G | A | 7 | a0001c0003t0138a0001c0009t0021a0001c0014t0059others(4): Show | 11 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9633G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9633 | chr3 | 133788253 | |||||
chr3:133788275
|
G | T | 101 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(98): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*9655G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 9655 | chr3 | 133788275 | |||||
chr3:133788638
|
TC | T | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(72): Show | 127 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*10021delC | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10021 | INFO_REALIGN_3_PRIME | chr3 | 133788638 | ||||
chr3:133788665
|
T | C | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(72): Show | 127 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*10045T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10045 | chr3 | 133788665 | |||||
chr3:133788685
|
C | T | 1 | a0002c0002t0105 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10065C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10065 | chr3 | 133788685 | |||||
chr3:133788694
|
A | C | 7 | a0001c0003t0138a0001c0009t0021a0001c0014t0059others(4): Show | 11 | HG02647.hp2 HG02896.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10074A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10074 | chr3 | 133788694 | |||||
chr3:133788696
|
G | A | 1 | a0001c0003t0122 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10076G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10076 | chr3 | 133788696 | |||||
chr3:133788812
|
G | A | 1 | a0001c0003t0150 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10192G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10192 | chr3 | 133788812 | |||||
chr3:133789059
|
G | C | 2 | a0001c0003t0224a0001c0003t0237 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10439G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10439 | chr3 | 133789059 | |||||
chr3:133789083
|
C | T | 1 | a0001c0003t0127 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10463C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10463 | chr3 | 133789083 | |||||
chr3:133789271
|
C | T | 1 | a0002c0002t0174 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10651C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10651 | chr3 | 133789271 | |||||
chr3:133789380
|
C | T | 3 | a0001c0001t0054a0001c0001t0232a0001c0001t0236 | 4 | HG02602.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10760C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10760 | chr3 | 133789380 | |||||
chr3:133789389
|
G | T | 24 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(21): Show | 28 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*10769G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10769 | chr3 | 133789389 | |||||
chr3:133789456
|
T | C | 101 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(98): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*10836T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 10836 | chr3 | 133789456 | |||||
chr3:133789620
|
A | T | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(74): Show | 129 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*11000A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11000 | chr3 | 133789620 | |||||
chr3:133789707
|
G | A | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(74): Show | 129 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*11087G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11087 | chr3 | 133789707 | |||||
chr3:133789747
|
C | A | 4 | a0001c0003t0138a0001c0014t0059a0001c0015t0267others(1): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11127C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11127 | chr3 | 133789747 | |||||
chr3:133789879
|
G | A | 6 | a0002c0002t0041a0002c0002t0087a0002c0002t0176others(3): Show | 6 | HG02486.hp1 HG02698.hp1 HG03688.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11259G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11259 | chr3 | 133789879 | |||||
chr3:133789879
|
G | GT | 25 | a0001c0003t0115a0001c0003t0116a0001c0003t0138others(22): Show | 29 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*11288dupT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11289 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
G | GTT | 9 | a0001c0001t0226a0001c0003t0147a0001c0005t0130others(6): Show | 9 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*11287_*11288dupTT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11289 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
G | GTTT | 11 | a0001c0003t0024a0001c0003t0056a0001c0003t0139others(8): Show | 15 | HG00423.hp2 HG01081.hp2 HG01496.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*11286_*11288dupTT others(1): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11289 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
G | GTTTT | 10 | a0001c0001t0025a0001c0001t0049a0001c0001t0252others(7): Show | 12 | HG00735.hp2 HG00741.hp1 HG01257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*11285_*11288dupTT others(2): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11289 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GT | G | 38 | a0001c0003t0039a0001c0003t0224a0001c0004t0004others(35): Show | 55 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*11288delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11288 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTT | G | 11 | a0001c0003t0023a0001c0003t0148a0001c0003t0150others(8): Show | 12 | HG01243.hp2 HG01515.hp2 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*11287_*11288delTT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11287 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTTTTTTT others(1): Show |
G | 7 | a0001c0006t0044a0001c0006t0045a0001c0006t0111others(4): Show | 9 | HG01123.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*11281_*11288delTT others(6): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11281 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTTTTTTT others(2): Show |
G | 25 | a0001c0001t0054a0001c0001t0222a0001c0001t0223others(22): Show | 29 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*11280_*11288delTT others(7): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11280 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTTTTTTT others(3): Show |
G | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(58): Show | 112 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*11279_*11288delTT others(8): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11279 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTTTTTTT others(4): Show |
G | 8 | a0001c0001t0229a0001c0001t0238a0001c0001t0242others(5): Show | 9 | HG01257.hp1 HG02056.hp2 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*11278_*11288delTT others(9): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11278 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTTTTTTT others(5): Show |
G | 38 | a0001c0001t0249a0001c0005t0071a0002c0002t0003others(35): Show | 58 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*11277_*11288delTT others(10): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11277 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789879
|
GTTTTTTT others(8): Show |
G | 1 | a0003c0008t0199 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11274_*11288delTT others(13): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11274 | INFO_REALIGN_3_PRIME | chr3 | 133789879 | ||||
chr3:133789880
|
T | A | 2 | a0002c0002t0042a0002c0012t0042 | 2 | HG03834.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11260T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11260 | chr3 | 133789880 | |||||
chr3:133789897
|
T | G | 1 | a0001c0003t0112 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11277T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11277 | chr3 | 133789897 | |||||
chr3:133789901
|
T | G | 1 | a0001c0003t0112 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11281T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11281 | chr3 | 133789901 | |||||
chr3:133789920
|
A | G | 1 | a0002c0002t0180 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11300A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11300 | chr3 | 133789920 | |||||
chr3:133789964
|
C | T | 4 | a0001c0003t0138a0001c0014t0059a0001c0015t0267others(1): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11344C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11344 | chr3 | 133789964 | |||||
chr3:133790098
|
C | T | 2 | a0001c0003t0224a0001c0003t0237 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11478C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11478 | chr3 | 133790098 | |||||
chr3:133790454
|
A | T | 1 | a0002c0012t0175 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11834A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11834 | chr3 | 133790454 | |||||
chr3:133790591
|
T | C | 1 | a0002c0002t0100 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11971T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11971 | chr3 | 133790591 | |||||
chr3:133790614
|
G | A | 1 | a0001c0003t0112 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11994G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 11994 | chr3 | 133790614 | |||||
chr3:133790640
|
G | T | 1 | a0001c0005t0134 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12020G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12020 | chr3 | 133790640 | |||||
chr3:133790726
|
C | A | 3 | a0001c0003t0023a0001c0003t0181a0008c0023t0023 | 4 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*12106C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12106 | chr3 | 133790726 | |||||
chr3:133790808
|
T | C | 4 | a0001c0003t0138a0001c0014t0059a0001c0015t0267others(1): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12188T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12188 | chr3 | 133790808 | |||||
chr3:133791060
|
T | A | 4 | a0001c0003t0023a0001c0003t0122a0001c0003t0181others(1): Show | 5 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12440T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12440 | chr3 | 133791060 | |||||
chr3:133791061
|
A | T | 1 | a0001c0003t0265 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12441A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12441 | chr3 | 133791061 | |||||
chr3:133791322
|
G | A | 23 | a0001c0005t0071a0002c0002t0003a0002c0002t0009others(20): Show | 39 | HG00544.hp1 HG00621.hp2 HG01081.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*12702G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12702 | chr3 | 133791322 | |||||
chr3:133791546
|
T | C | 1 | a0001c0006t0191 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12926T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12926 | chr3 | 133791546 | |||||
chr3:133791569
|
G | A | 101 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(98): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*12949G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 12949 | chr3 | 133791569 | |||||
chr3:133791780
|
G | A | 14 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(11): Show | 17 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*13160G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13160 | chr3 | 133791780 | |||||
chr3:133791791
|
T | C | 1 | a0001c0006t0191 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13171T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13171 | chr3 | 133791791 | |||||
chr3:133792088
|
C | T | 14 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(11): Show | 17 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*13468C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13468 | chr3 | 133792088 | |||||
chr3:133792319
|
G | A | 1 | a0001c0003t0122 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13699G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13699 | chr3 | 133792319 | |||||
chr3:133792463
|
C | A | 214 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(211): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*13843C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13843 | chr3 | 133792463 | |||||
chr3:133792572
|
C | G | 1 | a0002c0002t0174 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13952C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13952 | chr3 | 133792572 | |||||
chr3:133792597
|
C | T | 4 | a0001c0004t0159a0001c0004t0168a0001c0004t0266others(1): Show | 4 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*13977C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 13977 | chr3 | 133792597 | |||||
chr3:133792662
|
C | T | 2 | a0001c0001t0049a0001c0003t0049 | 2 | HG00741.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14042C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 14042 | chr3 | 133792662 | |||||
chr3:133792949
|
G | A | 1 | a0001c0003t0139 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14329G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 14329 | chr3 | 133792949 | |||||
chr3:133793234
|
T | A | 214 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(211): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*14614T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 14614 | chr3 | 133793234 | |||||
chr3:133793491
|
G | T | 2 | a0001c0005t0083a0001c0024t0169 | 2 | HG00642.hp1 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14871G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 14871 | chr3 | 133793491 | |||||
chr3:133793499
|
GAA | G | 24 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(21): Show | 28 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*14885_*14886delAA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 14885 | INFO_REALIGN_3_PRIME | chr3 | 133793499 | ||||
chr3:133793635
|
T | C | 2 | a0001c0003t0224a0001c0003t0237 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15015T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15015 | chr3 | 133793635 | |||||
chr3:133793861
|
T | C | 1 | a0002c0002t0087 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15241T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15241 | chr3 | 133793861 | |||||
chr3:133794056
|
T | G | 1 | a0002c0002t0108 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15436T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15436 | chr3 | 133794056 | |||||
chr3:133794065
|
A | G | 1 | a0001c0001t0058 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*15445A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15445 | chr3 | 133794065 | |||||
chr3:133794138
|
G | A | 2 | a0001c0003t0224a0001c0003t0237 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15518G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15518 | chr3 | 133794138 | |||||
chr3:133794186
|
G | A | 1 | a0001c0003t0127 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15566G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15566 | chr3 | 133794186 | |||||
chr3:133794192
|
G | T | 1 | a0001c0005t0081 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15572G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15572 | chr3 | 133794192 | |||||
chr3:133794232
|
G | A | 2 | a0001c0003t0224a0001c0003t0237 | 2 | NA19030.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15612G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15612 | chr3 | 133794232 | |||||
chr3:133794582
|
A | G | 1 | a0001c0003t0248 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15962A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15962 | chr3 | 133794582 | |||||
chr3:133794608
|
C | A | 2 | a0001c0006t0046a0001c0006t0140 | 3 | HG02717.hp2 HG02723.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*15988C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 15988 | chr3 | 133794608 | |||||
chr3:133794705
|
T | C | 2 | a0001c0005t0077a0001c0005t0084 | 2 | HG00621.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16085T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16085 | chr3 | 133794705 | |||||
chr3:133794945
|
G | A | 3 | a0001c0003t0023a0001c0003t0181a0008c0023t0023 | 4 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*16325G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16325 | chr3 | 133794945 | |||||
chr3:133795346
|
C | T | 101 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(98): Show | 131 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*16726C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16726 | chr3 | 133795346 | |||||
chr3:133795372
|
C | T | 1 | a0001c0001t0255 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16752C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16752 | chr3 | 133795372 | |||||
chr3:133795454
|
C | T | 1 | a0001c0001t0247 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16834C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16834 | chr3 | 133795454 | |||||
chr3:133795455
|
G | A | 2 | a0001c0003t0039a0001c0004t0039 | 2 | HG02040.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16835G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16835 | chr3 | 133795455 | |||||
chr3:133795470
|
T | A | 239 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(236): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*16850T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16850 | chr3 | 133795470 | |||||
chr3:133795570
|
A | AT | 14 | a0001c0001t0245a0001c0001t0250a0001c0003t0138others(11): Show | 15 | HG00621.hp1 HG01175.hp1 HG02647.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*16973dupT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16974 | INFO_REALIGN_3_PRIME | chr3 | 133795570 | ||||
chr3:133795570
|
A | ATT | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(36): Show | 75 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*16972_*16973dupTT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16974 | INFO_REALIGN_3_PRIME | chr3 | 133795570 | ||||
chr3:133795570
|
A | ATTT | 28 | a0001c0001t0005a0001c0001t0008a0001c0001t0011others(25): Show | 44 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*16971_*16973dupTT others(1): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16974 | INFO_REALIGN_3_PRIME | chr3 | 133795570 | ||||
chr3:133795570
|
AT | A | 111 | a0001c0001t0025a0001c0001t0049a0001c0001t0226others(108): Show | 144 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*16973delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16973 | INFO_REALIGN_3_PRIME | chr3 | 133795570 | ||||
chr3:133795618
|
C | T | 3 | a0001c0004t0018a0001c0004t0162a0001c0004t0165 | 5 | HG01168.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*16998C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16998 | chr3 | 133795618 | |||||
chr3:133795619
|
G | A | 222 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(219): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*16999G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 16999 | chr3 | 133795619 | |||||
chr3:133795639
|
G | A | 1 | a0001c0005t0084 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17019G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17019 | chr3 | 133795639 | |||||
chr3:133795644
|
C | T | 13 | a0001c0005t0016a0001c0005t0130a0001c0005t0131others(10): Show | 14 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*17024C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17024 | chr3 | 133795644 | |||||
chr3:133795676
|
C | T | 3 | a0001c0004t0168a0001c0005t0080a0006c0013t0167 | 3 | HG01070.hp2 HG01071.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17056C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17056 | chr3 | 133795676 | |||||
chr3:133795733
|
G | A | 1 | a0001c0003t0122 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17113G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17113 | chr3 | 133795733 | |||||
chr3:133795767
|
G | A | 15 | a0001c0001t0261a0001c0001t0262a0001c0003t0010others(12): Show | 18 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*17147G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17147 | chr3 | 133795767 | |||||
chr3:133795904
|
T | C | 13 | a0001c0005t0016a0001c0005t0130a0001c0005t0131others(10): Show | 14 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*17284T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17284 | chr3 | 133795904 | |||||
chr3:133795906
|
T | C | 4 | a0001c0001t0226a0001c0001t0252a0001c0001t0253others(1): Show | 5 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*17286T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17286 | chr3 | 133795906 | |||||
chr3:133795937
|
C | T | 14 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(11): Show | 17 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*17317C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17317 | chr3 | 133795937 | |||||
chr3:133795970
|
C | T | 1 | a0002c0002t0099 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17350C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17350 | chr3 | 133795970 | |||||
chr3:133795978
|
C | T | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(72): Show | 127 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*17358C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17358 | chr3 | 133795978 | |||||
chr3:133796136
|
G | A | 2 | a0001c0003t0147a0001c0005t0069 | 2 | HG02572.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*17516G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17516 | chr3 | 133796136 | |||||
chr3:133796377
|
G | A | 1 | a0001c0003t0150 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17757G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 17757 | chr3 | 133796377 | |||||
chr3:133796625
|
C | T | 14 | a0001c0003t0112a0001c0006t0044a0001c0006t0045others(11): Show | 17 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*18005C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 17/17 | 18005 | chr3 | 133796625 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:133746509
|
G | T | 14 | a0001c0001t0001g0003a0001c0001t0005g0003a0001c0001t0005g0252others(11): Show | 17 | HG01255.hp2 HG02080.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.43+26G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133746509 | ||||||
chr3:133746549
|
C | T | 2 | a0001c0001t0058g0244a0001c0001t0058g0245 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.43+66C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133746549 | ||||||
chr3:133746855
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 153 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.43+372T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133746855 | ||||||
chr3:133746861
|
C | G | 2 | a0006c0013t0143g0243a0006c0013t0167g0242 | 2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.43+378C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133746861 | ||||||
chr3:133747116
|
T | G | 1 | a0001c0001t0243g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.43+633T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747116 | ||||||
chr3:133747311
|
C | T | 24 | a0001c0001t0001g0232a0001c0003t0056g0051a0001c0003t0147g0241others(21): Show | 25 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.43+828C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747311 | ||||||
chr3:133747378
|
A | G | 30 | a0001c0001t0001g0232a0001c0003t0023g0025a0001c0003t0056g0051others(27): Show | 32 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.43+895A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747378 | ||||||
chr3:133747530
|
A | G | 78 | a0001c0001t0002g0183a0001c0001t0231g0210a0001c0001t0244g0215others(75): Show | 85 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.44-882A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747530 | ||||||
chr3:133747613
|
T | A | 30 | a0001c0001t0001g0232a0001c0003t0023g0025a0001c0003t0056g0051others(27): Show | 32 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.44-799T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747613 | ||||||
chr3:133747688
|
A | G | 4 | a0001c0006t0046g0179a0001c0006t0046g0180a0001c0006t0140g0178others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-724A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747688 | ||||||
chr3:133747744
|
A | G | 16 | a0001c0001t0005g0020a0001c0001t0011g0020a0001c0001t0049g0103others(13): Show | 18 | HG00140.hp2 HG00741.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-668A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747744 | ||||||
chr3:133747748
|
A | T | 1 | a0006c0013t0144g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.44-664A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747748 | ||||||
chr3:133747790
|
G | A | 1 | a0001c0003t0182g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.44-622G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747790 | ||||||
chr3:133747932
|
T | TA | 8 | a0001c0001t0245g0054a0001c0003t0112g0107a0001c0004t0163g0181others(5): Show | 8 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-467dupA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr3 | 133747932 | |||||
chr3:133747952
|
A | G | 1 | a0001c0004t0019g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.44-460A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747952 | ||||||
chr3:133747977
|
T | C | 1 | a0001c0015t0267g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.44-435T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133747977 | ||||||
chr3:133748041
|
G | A | 60 | a0001c0001t0002g0183a0001c0001t0231g0210a0001c0001t0244g0215others(57): Show | 65 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.44-371G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133748041 | ||||||
chr3:133748318
|
A | G | 1 | a0001c0015t0268g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.44-94A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 1/16 | chr3 | 133748318 | ||||||
chr3:133748598
|
G | C | 2 | a0001c0003t0057g0109a0001c0003t0148g0108 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.216+14G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133748598 | ||||||
chr3:133748600
|
C | T | 1 | a0001c0003t0007g0176 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.216+16C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133748600 | ||||||
chr3:133748673
|
G | A | 11 | a0001c0003t0010g0006a0001c0003t0034g0110a0001c0003t0034g0114others(8): Show | 13 | HG00099.hp2 HG00609.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.216+89G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133748673 | ||||||
chr3:133748852
|
C | T | 28 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(25): Show | 32 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.216+268C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133748852 | ||||||
chr3:133748935
|
G | A | 2 | a0001c0001t0252g0027a0001c0001t0253g0027 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.216+351G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133748935 | ||||||
chr3:133749029
|
T | C | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+445T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749029 | ||||||
chr3:133749068
|
G | A | 1 | a0001c0001t0026g0246 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.216+484G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749068 | ||||||
chr3:133749085
|
G | A | 1 | a0001c0005t0069g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.216+501G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749085 | ||||||
chr3:133749086
|
G | A | 4 | a0003c0008t0206g0026a0003c0008t0207g0026a0003c0008t0209g0026others(1): Show | 4 | HG00280.hp2 HG00323.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+502G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749086 | ||||||
chr3:133749087
|
G | A | 3 | a0001c0007t0017g0019a0001c0007t0038g0019a0001c0007t0156g0019 | 3 | NA18953.hp1 NA18973.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.216+503G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749087 | ||||||
chr3:133749101
|
C | T | 11 | a0001c0005t0016g0009a0001c0005t0016g0037a0001c0005t0068g0095others(8): Show | 11 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+517C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749101 | ||||||
chr3:133749151
|
G | A | 1 | a0001c0015t0267g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.216+567G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749151 | ||||||
chr3:133749168
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(152): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.216+584A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749168 | ||||||
chr3:133749295
|
G | A | 60 | a0001c0003t0070g0121a0001c0003t0115g0137a0001c0003t0116g0123others(57): Show | 67 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.216+711G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749295 | ||||||
chr3:133749462
|
A | G | 2 | a0001c0003t0147g0241a0001c0003t0237g0240 | 2 | HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.216+878A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749462 | ||||||
chr3:133749581
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.216+997A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749581 | ||||||
chr3:133749855
|
G | A | 1 | a0001c0003t0049g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.216+1271G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749855 | ||||||
chr3:133749894
|
C | T | 1 | a0001c0001t0006g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.216+1310C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749894 | ||||||
chr3:133749985
|
G | T | 9 | a0001c0006t0045g0030a0001c0006t0151g0057a0001c0006t0183g0061others(6): Show | 10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+1401G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133749985 | ||||||
chr3:133750005
|
G | A | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+1421G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750005 | ||||||
chr3:133750021
|
A | G | 1 | a0002c0002t0014g0150 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.216+1437A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750021 | ||||||
chr3:133750392
|
G | A | 1 | a0001c0007t0154g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.216+1808G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750392 | ||||||
chr3:133750458
|
T | TCCTCCTC others(3): Show |
320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(317): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.216+1876_216+1877i others(12): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133750458 | |||||
chr3:133750480
|
C | G | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+1896C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750480 | ||||||
chr3:133750587
|
G | A | 13 | a0001c0006t0045g0030a0001c0006t0046g0179a0001c0006t0046g0180others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.216+2003G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750587 | ||||||
chr3:133750666
|
C | G | 5 | a0001c0001t0002g0014a0001c0001t0002g0092a0001c0001t0239g0091others(2): Show | 6 | HG01255.hp1 HG01943.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+2082C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750666 | ||||||
chr3:133750666
|
C | T | 3 | a0001c0005t0074g0174a0001c0005t0075g0173a0001c0005t0076g0175 | 3 | HG01099.hp2 HG01515.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.216+2082C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750666 | ||||||
chr3:133750686
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 119 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.216+2102G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750686 | ||||||
chr3:133750740
|
A | C | 5 | a0003c0008t0206g0026a0003c0008t0207g0026a0003c0008t0208g0090others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2156A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750740 | ||||||
chr3:133750774
|
T | A | 2 | a0001c0001t0002g0031a0001c0001t0008g0064 | 3 | HG00544.hp2 NA18612.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.216+2190T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750774 | ||||||
chr3:133750779
|
A | T | 64 | a0001c0003t0070g0121a0001c0003t0115g0137a0001c0003t0116g0123others(61): Show | 73 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.216+2195A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750779 | ||||||
chr3:133750781
|
T | A | 3 | a0001c0001t0008g0065a0001c0001t0026g0247a0001c0015t0268g0230 | 3 | NA18943.hp2 NA18960.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.216+2197T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750781 | ||||||
chr3:133750782
|
A | G | 1 | a0001c0004t0002g0214 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.216+2198A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750782 | ||||||
chr3:133750786
|
A | G | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2202A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133750786 | ||||||
chr3:133751011
|
G | C | 33 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(30): Show | 39 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.216+2427G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751011 | ||||||
chr3:133751131
|
A | G | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-2464A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751131 | ||||||
chr3:133751181
|
A | G | 57 | a0001c0001t0026g0253a0001c0001t0231g0210a0001c0003t0248g0208others(54): Show | 62 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.217-2414A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751181 | ||||||
chr3:133751224
|
T | C | 4 | a0002c0002t0015g0117a0002c0002t0103g0119a0002c0002t0104g0118others(1): Show | 4 | NA18993.hp1 NA19005.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-2371T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751224 | ||||||
chr3:133751229
|
CT | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(292): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.217-2345delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133751229 | |||||
chr3:133751229
|
CTT | C | 8 | a0001c0001t0232g0098a0001c0001t0242g0099a0001c0003t0070g0121others(5): Show | 8 | HG01168.hp2 HG01257.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-2346_217-2345d others(4): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133751229 | |||||
chr3:133751263
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 119 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.217-2332C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751263 | ||||||
chr3:133751295
|
C | T | 30 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(27): Show | 34 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.217-2300C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751295 | ||||||
chr3:133751301
|
C | T | 1 | a0001c0005t0076g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.217-2294C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751301 | ||||||
chr3:133751302
|
G | A | 31 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(28): Show | 35 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.217-2293G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751302 | ||||||
chr3:133751342
|
C | T | 5 | a0003c0008t0206g0026a0003c0008t0207g0026a0003c0008t0208g0090others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-2253C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751342 | ||||||
chr3:133751382
|
G | A | 4 | a0001c0003t0023g0025a0001c0003t0181g0025a0001c0003t0182g0227others(1): Show | 5 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-2213G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751382 | ||||||
chr3:133751444
|
T | G | 92 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(89): Show | 105 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.217-2151T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751444 | ||||||
chr3:133751719
|
C | T | 1 | a0001c0006t0149g0089 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217-1876C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133751719 | ||||||
chr3:133752027
|
A | G | 1 | a0001c0015t0268g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217-1568A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752027 | ||||||
chr3:133752065
|
A | G | 28 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(25): Show | 32 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.217-1530A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752065 | ||||||
chr3:133752097
|
AT | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(252): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.217-1481delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133752097 | |||||
chr3:133752097
|
ATT | A | 59 | a0001c0001t0239g0091a0001c0003t0010g0006a0001c0003t0011g0047others(56): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.217-1482_217-1481d others(4): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133752097 | |||||
chr3:133752195
|
C | T | 1 | a0001c0003t0148g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.217-1400C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752195 | ||||||
chr3:133752196
|
G | A | 28 | a0001c0003t0056g0051a0001c0003t0212g0239a0001c0006t0149g0089others(25): Show | 30 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.217-1399G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752196 | ||||||
chr3:133752453
|
G | A | 1 | a0001c0003t0139g0219 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.217-1142G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752453 | ||||||
chr3:133752498
|
A | G | 1 | a0001c0015t0268g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217-1097A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752498 | ||||||
chr3:133752595
|
TATA | T | 31 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(28): Show | 35 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.217-996_217-994del others(3): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133752595 | |||||
chr3:133752736
|
T | G | 1 | a0001c0003t0127g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.217-859T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133752736 | ||||||
chr3:133753010
|
A | C | 1 | a0001c0015t0268g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217-585A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753010 | ||||||
chr3:133753067
|
AT | A | 3 | a0001c0001t0054g0038a0001c0001t0232g0098a0001c0001t0236g0100 | 4 | HG02602.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-527delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753067 | ||||||
chr3:133753096
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.217-499C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753096 | ||||||
chr3:133753193
|
G | C | 4 | a0001c0003t0070g0121a0001c0003t0138g0125a0002c0002t0033g0039others(1): Show | 5 | HG03471.hp2 HG03579.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-402G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753193 | ||||||
chr3:133753204
|
C | G | 1 | a0001c0004t0172g0211 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.217-391C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753204 | ||||||
chr3:133753313
|
G | A | 3 | a0001c0003t0034g0110a0001c0003t0120g0112a0001c0003t0121g0111 | 3 | HG00735.hp2 HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.217-282G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753313 | ||||||
chr3:133753358
|
G | A | 2 | a0001c0003t0057g0109a0001c0003t0148g0108 | 2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.217-237G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753358 | ||||||
chr3:133753383
|
A | C | 94 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(91): Show | 107 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.217-212A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | chr3 | 133753383 | ||||||
chr3:133753440
|
CAG | C | 33 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(30): Show | 37 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.217-152_217-151del others(2): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 133753440 | |||||
chr3:133753921
|
G | A | 1 | a0001c0003t0119g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325+218G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133753921 | ||||||
chr3:133753931
|
C | G | 91 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(88): Show | 102 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+228C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133753931 | ||||||
chr3:133754053
|
G | A | 91 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(88): Show | 102 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+350G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754053 | ||||||
chr3:133754114
|
G | A | 52 | a0001c0003t0248g0208a0001c0004t0001g0016a0001c0004t0001g0202others(49): Show | 57 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.326-381G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754114 | ||||||
chr3:133754152
|
T | C | 2 | a0001c0004t0204g0046a0001c0004t0205g0046 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.326-343T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754152 | ||||||
chr3:133754211
|
G | A | 1 | a0001c0007t0153g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.326-284G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754211 | ||||||
chr3:133754261
|
G | A | 58 | a0001c0003t0070g0121a0001c0003t0115g0137a0001c0003t0116g0123others(55): Show | 65 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.326-234G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754261 | ||||||
chr3:133754414
|
C | A | 2 | a0001c0001t0055g0101a0001c0001t0057g0102 | 2 | HG01433.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.326-81C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754414 | ||||||
chr3:133754428
|
C | T | 17 | a0001c0006t0044g0048a0001c0006t0044g0229a0001c0006t0045g0030others(14): Show | 18 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.326-67C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754428 | ||||||
chr3:133754431
|
T | A | 1 | a0001c0005t0012g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.326-64T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754431 | ||||||
chr3:133754472
|
C | G | 1 | a0001c0015t0267g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326-23C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 3/16 | chr3 | 133754472 | ||||||
chr3:133754681
|
C | A | 2 | a0001c0004t0020g0186a0001c0004t0171g0189 | 2 | NA18942.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.502+10C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754681 | ||||||
chr3:133754781
|
G | T | 29 | a0001c0003t0056g0051a0001c0003t0212g0239a0001c0006t0149g0089others(26): Show | 31 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.502+110G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754781 | ||||||
chr3:133754799
|
G | A | 58 | a0001c0003t0070g0121a0001c0003t0115g0137a0001c0003t0116g0123others(55): Show | 65 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.502+128G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754799 | ||||||
chr3:133754898
|
G | C | 33 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(30): Show | 37 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.502+227G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754898 | ||||||
chr3:133754923
|
T | A | 17 | a0001c0006t0044g0048a0001c0006t0044g0229a0001c0006t0045g0030others(14): Show | 18 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.502+252T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754923 | ||||||
chr3:133754925
|
G | A | 1 | a0002c0002t0032g0127 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.502+254G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754925 | ||||||
chr3:133754938
|
A | T | 1 | a0001c0004t0040g0209 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.502+267A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754938 | ||||||
chr3:133754990
|
G | T | 17 | a0002c0002t0041g0049a0002c0002t0042g0234a0002c0002t0173g0236others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.502+319G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133754990 | ||||||
chr3:133755101
|
T | G | 28 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(25): Show | 32 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.503-262T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133755101 | ||||||
chr3:133755159
|
C | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 128 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.503-204C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133755159 | ||||||
chr3:133755257
|
T | C | 1 | a0001c0001t0005g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.503-106T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133755257 | ||||||
chr3:133755303
|
T | G | 33 | a0001c0003t0010g0006a0001c0003t0011g0047a0001c0003t0024g0011others(30): Show | 37 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.503-60T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 4/16 | chr3 | 133755303 | ||||||
chr3:133755508
|
T | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0002g0005others(5): Show | 12 | HG00544.hp2 HG02523.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.635+13T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133755508 | ||||||
chr3:133755674
|
C | G | 1 | a0002c0002t0107g0149 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.635+179C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133755674 | ||||||
chr3:133755763
|
G | A | 56 | a0001c0003t0070g0121a0001c0003t0115g0137a0001c0003t0116g0123others(53): Show | 62 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.635+268G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133755763 | ||||||
chr3:133755898
|
T | A | 1 | a0002c0002t0174g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.636-384T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133755898 | ||||||
chr3:133755981
|
T | C | 1 | a0001c0009t0016g0056 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.636-301T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133755981 | ||||||
chr3:133755988
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 128 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.636-294T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133755988 | ||||||
chr3:133756114
|
C | T | 17 | a0001c0006t0044g0048a0001c0006t0044g0229a0001c0006t0045g0030others(14): Show | 18 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.636-168C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133756114 | ||||||
chr3:133756169
|
G | A | 1 | a0001c0007t0004g0088 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.636-113G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133756169 | ||||||
chr3:133756181
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.636-101C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 5/16 | chr3 | 133756181 | ||||||
chr3:133756407
|
T | C | 1 | a0001c0001t0238g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.691+70T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 6/16 | chr3 | 133756407 | ||||||
chr3:133756491
|
C | T | 6 | a0001c0003t0024g0011a0001c0003t0139g0219a0001c0003t0193g0224others(3): Show | 8 | HG01928.hp2 HG01952.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.691+154C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 6/16 | chr3 | 133756491 | ||||||
chr3:133756591
|
G | A | 13 | a0001c0006t0044g0048a0001c0006t0044g0229a0001c0006t0045g0030others(10): Show | 14 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.692-240G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 6/16 | chr3 | 133756591 | ||||||
chr3:133756685
|
G | A | 4 | a0001c0001t0058g0244a0001c0001t0058g0245a0001c0001t0261g0068others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.692-146G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 6/16 | chr3 | 133756685 | ||||||
chr3:133756719
|
G | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(222): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.692-112G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 6/16 | chr3 | 133756719 | ||||||
chr3:133756770
|
G | C | 4 | a0001c0003t0023g0025a0001c0003t0181g0025a0001c0003t0182g0227others(1): Show | 5 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.692-61G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 6/16 | chr3 | 133756770 | ||||||
chr3:133757117
|
A | G | 27 | a0001c0001t0252g0027a0001c0001t0253g0027a0001c0006t0044g0048others(24): Show | 29 | HG01123.hp2 HG01891.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.870+108A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757117 | ||||||
chr3:133757206
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+197C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757206 | ||||||
chr3:133757239
|
G | A | 54 | a0001c0001t0025g0032a0001c0004t0001g0016a0001c0004t0001g0202others(51): Show | 60 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.870+230G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757239 | ||||||
chr3:133757308
|
A | G | 1 | a0001c0001t0050g0251 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.870+299A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757308 | ||||||
chr3:133757369
|
G | A | 1 | a0001c0003t0237g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870+360G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757369 | ||||||
chr3:133757483
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(317): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.871-286T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757483 | ||||||
chr3:133757549
|
G | A | 1 | a0001c0001t0263g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.871-220G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757549 | ||||||
chr3:133757570
|
G | A | 8 | a0001c0001t0051g0083a0001c0001t0051g0085a0001c0007t0017g0019others(5): Show | 8 | NA18951.hp1 NA18953.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-199G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757570 | ||||||
chr3:133757577
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(206): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.871-192C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757577 | ||||||
chr3:133757609
|
G | T | 1 | a0001c0001t0259g0082 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.871-160G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757609 | ||||||
chr3:133757724
|
C | CACTGAGT others(5): Show |
1 | a0001c0001t0051g0083 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.871-45_871-44insAC others(10): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757724 | ||||||
chr3:133757726
|
T | C | 1 | a0001c0001t0051g0083 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.871-43T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757726 | ||||||
chr3:133757727
|
T | A | 1 | a0001c0001t0051g0083 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.871-42T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 7/16 | chr3 | 133757727 | ||||||
chr3:133758008
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1048+62C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133758008 | ||||||
chr3:133758364
|
A | G | 1 | a0001c0001t0239g0091 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1048+418A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133758364 | ||||||
chr3:133758756
|
G | T | 9 | a0002c0002t0041g0049a0002c0002t0042g0234a0002c0002t0087g0169others(6): Show | 9 | HG02486.hp1 HG02698.hp1 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-419G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133758756 | ||||||
chr3:133758857
|
T | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1049-318T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133758857 | ||||||
chr3:133758903
|
G | A | 1 | a0001c0001t0259g0082 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1049-272G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133758903 | ||||||
chr3:133758977
|
A | C | 1 | a0001c0005t0081g0168 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1049-198A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133758977 | ||||||
chr3:133759013
|
G | A | 1 | a0001c0004t0142g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1049-162G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133759013 | ||||||
chr3:133759117
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1049-58C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 8/16 | chr3 | 133759117 | ||||||
chr3:133759411
|
T | C | 1 | a0001c0001t0232g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1203+82T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133759411 | ||||||
chr3:133759470
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203+141C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133759470 | ||||||
chr3:133759510
|
G | A | 3 | a0006c0013t0143g0243a0006c0013t0144g0226a0006c0013t0167g0242 | 3 | HG01070.hp2 HG01074.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1203+181G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133759510 | ||||||
chr3:133759713
|
T | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 216 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.1203+384T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133759713 | ||||||
chr3:133759883
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1203+554G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133759883 | ||||||
chr3:133760215
|
A | G | 5 | a0001c0003t0224g0217a0001c0003t0265g0216a0005c0011t0021g0018others(2): Show | 7 | HG02486.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203+886A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760215 | ||||||
chr3:133760287
|
T | A | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1203+958T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760287 | ||||||
chr3:133760346
|
G | A | 4 | a0001c0003t0023g0025a0001c0003t0181g0025a0001c0003t0182g0227others(1): Show | 5 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203+1017G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760346 | ||||||
chr3:133760356
|
G | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(317): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1203+1027G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760356 | ||||||
chr3:133760386
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1203+1057A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760386 | ||||||
chr3:133760598
|
G | C | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203+1269G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760598 | ||||||
chr3:133760655
|
T | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1203+1326T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760655 | ||||||
chr3:133760782
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 124 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1203+1453C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760782 | ||||||
chr3:133760799
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203+1470C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760799 | ||||||
chr3:133760884
|
G | A | 1 | a0001c0006t0191g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1203+1555G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760884 | ||||||
chr3:133760893
|
T | C | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203+1564T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133760893 | ||||||
chr3:133761105
|
C | G | 1 | a0001c0004t0163g0181 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1203+1776C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761105 | ||||||
chr3:133761131
|
A | G | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1203+1802A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761131 | ||||||
chr3:133761177
|
C | T | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1203+1848C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761177 | ||||||
chr3:133761330
|
C | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1203+2001C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761330 | ||||||
chr3:133761348
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1203+2019C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761348 | ||||||
chr3:133761393
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203+2064C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761393 | ||||||
chr3:133761432
|
G | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1203+2103G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761432 | ||||||
chr3:133761493
|
C | T | 9 | a0001c0004t0204g0046a0001c0004t0205g0046a0003c0008t0114g0172others(6): Show | 9 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1203+2164C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761493 | ||||||
chr3:133761543
|
C | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1203+2214C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761543 | ||||||
chr3:133761544
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1203+2215T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761544 | ||||||
chr3:133761614
|
T | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(111): Show | 135 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1203+2285T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761614 | ||||||
chr3:133761744
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1203+2415A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761744 | ||||||
chr3:133761808
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1204-2374G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761808 | ||||||
chr3:133761892
|
C | T | 3 | a0002c0002t0003g0144a0002c0002t0013g0145a0002c0002t0031g0146 | 3 | HG00544.hp1 HG02056.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1204-2290C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761892 | ||||||
chr3:133761973
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1204-2209A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761973 | ||||||
chr3:133761986
|
G | A | 1 | a0001c0001t0223g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1204-2196G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133761986 | ||||||
chr3:133762119
|
C | G | 1 | a0003c0016t0198g0231 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1204-2063C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762119 | ||||||
chr3:133762284
|
T | C | 155 | a0001c0003t0023g0025a0001c0003t0070g0121a0001c0003t0115g0137others(152): Show | 165 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.1204-1898T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762284 | ||||||
chr3:133762299
|
G | C | 1 | a0001c0015t0268g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1204-1883G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762299 | ||||||
chr3:133762333
|
C | G | 1 | a0001c0005t0146g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1204-1849C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762333 | ||||||
chr3:133762372
|
C | A | 6 | a0001c0001t0005g0020a0001c0001t0011g0020a0001c0001t0055g0101others(3): Show | 7 | HG00140.hp2 HG01123.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1204-1810C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762372 | ||||||
chr3:133762391
|
G | A | 1 | a0001c0003t0121g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1204-1791G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762391 | ||||||
chr3:133762452
|
G | C | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1204-1730G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762452 | ||||||
chr3:133762654
|
G | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1204-1528G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762654 | ||||||
chr3:133762787
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0250g0073 | 2 | NA18940.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1204-1395G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762787 | ||||||
chr3:133762874
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1204-1308C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133762874 | ||||||
chr3:133763072
|
C | A | 3 | a0002c0012t0041g0070a0002c0012t0042g0071a0002c0012t0175g0053 | 3 | HG02698.hp1 HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1204-1110C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763072 | ||||||
chr3:133763162
|
T | G | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-1020T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763162 | ||||||
chr3:133763198
|
G | T | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1204-984G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763198 | ||||||
chr3:133763286
|
T | C | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1204-896T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763286 | ||||||
chr3:133763386
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 126 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1204-796G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763386 | ||||||
chr3:133763700
|
T | G | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1204-482T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763700 | ||||||
chr3:133763837
|
C | T | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1204-345C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763837 | ||||||
chr3:133763962
|
G | A | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1204-220G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133763962 | ||||||
chr3:133764026
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(103): Show | 125 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1204-156G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133764026 | ||||||
chr3:133764045
|
T | G | 44 | a0001c0005t0012g0023a0001c0005t0012g0153a0001c0005t0012g0166others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1204-137T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 9/16 | chr3 | 133764045 | ||||||
chr3:133764349
|
T | C | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1297+74T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 10/16 | chr3 | 133764349 | ||||||
chr3:133764726
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1298-149A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 10/16 | chr3 | 133764726 | ||||||
chr3:133764749
|
T | C | 1 | a0001c0001t0221g0074 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1298-126T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 10/16 | chr3 | 133764749 | ||||||
chr3:133764838
|
G | A | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1298-37G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 10/16 | chr3 | 133764838 | ||||||
chr3:133764852
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(154): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1298-23T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 10/16 | chr3 | 133764852 | ||||||
chr3:133765185
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(108): Show | 132 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1330+278G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765185 | ||||||
chr3:133765222
|
T | C | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1330+315T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765222 | ||||||
chr3:133765344
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0066others(63): Show | 79 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1330+437C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765344 | ||||||
chr3:133765429
|
C | T | 1 | a0001c0005t0012g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1330+522C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765429 | ||||||
chr3:133765492
|
T | C | 1 | a0001c0003t0112g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1330+585T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765492 | ||||||
chr3:133765496
|
C | G | 1 | a0002c0022t0101g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1330+589C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765496 | ||||||
chr3:133765549
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 140 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.1330+642T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765549 | ||||||
chr3:133765550
|
G | A | 4 | a0001c0003t0112g0107a0001c0003t0224g0217a0001c0003t0265g0216others(1): Show | 4 | HG02486.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1330+643G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765550 | ||||||
chr3:133765808
|
A | G | 2 | a0002c0002t0088g0142a0002c0002t0096g0141 | 2 | NA18951.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1331-470A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765808 | ||||||
chr3:133765867
|
AG | A | 4 | a0001c0003t0112g0107a0001c0003t0224g0217a0001c0003t0265g0216others(1): Show | 4 | HG02486.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331-410delG | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765867 | ||||||
chr3:133765868
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(112): Show | 136 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1331-410G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765868 | ||||||
chr3:133765869
|
T | A | 4 | a0001c0003t0112g0107a0001c0003t0224g0217a0001c0003t0265g0216others(1): Show | 4 | HG02486.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331-409T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765869 | ||||||
chr3:133765897
|
A | T | 3 | a0001c0004t0019g0045a0001c0004t0159g0192a0001c0004t0168g0045 | 3 | HG00140.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1331-381A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765897 | ||||||
chr3:133765986
|
T | C | 13 | a0001c0001t0025g0032a0001c0003t0024g0011a0001c0003t0025g0221others(10): Show | 16 | HG00423.hp2 HG01081.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1331-292T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133765986 | ||||||
chr3:133766060
|
A | C | 2 | a0001c0001t0005g0034a0001c0001t0230g0034 | 2 | HG00099.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1331-218A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133766060 | ||||||
chr3:133766154
|
G | A | 1 | a0001c0001t0261g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1331-124G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133766154 | ||||||
chr3:133766220
|
A | G | 1 | a0001c0005t0137g0096 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1331-58A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 11/16 | chr3 | 133766220 | ||||||
chr3:133766515
|
A | T | 2 | a0001c0003t0112g0107a0001c0006t0191g0062 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1486+82A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766515 | ||||||
chr3:133766527
|
G | C | 44 | a0001c0005t0012g0023a0001c0005t0012g0153a0001c0005t0012g0166others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1486+94G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766527 | ||||||
chr3:133766581
|
T | C | 1 | a0001c0005t0073g0158 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1486+148T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766581 | ||||||
chr3:133766610
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(176): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1486+177A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766610 | ||||||
chr3:133766806
|
T | C | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1486+373T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766806 | ||||||
chr3:133766827
|
T | A | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486+394T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766827 | ||||||
chr3:133766841
|
G | A | 5 | a0001c0003t0224g0217a0001c0003t0265g0216a0005c0011t0021g0018others(2): Show | 7 | HG02486.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486+408G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766841 | ||||||
chr3:133766986
|
C | T | 67 | a0001c0005t0012g0023a0001c0005t0012g0153a0001c0005t0012g0166others(64): Show | 68 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1486+553C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133766986 | ||||||
chr3:133767249
|
G | A | 76 | a0001c0001t0058g0244a0001c0001t0058g0245a0001c0001t0261g0068others(73): Show | 79 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1487-780G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133767249 | ||||||
chr3:133767776
|
G | A | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487-253G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133767776 | ||||||
chr3:133767850
|
A | G | 1 | a0001c0005t0068g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1487-179A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133767850 | ||||||
chr3:133768010
|
C | T | 1 | a0001c0014t0059g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1487-19C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 12/16 | chr3 | 133768010 | ||||||
chr3:133768176
|
A | C | 2 | a0001c0003t0011g0047a0001c0003t0055g0047 | 2 | HG00733.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1622+12A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133768176 | ||||||
chr3:133768268
|
G | A | 1 | a0001c0017t0028g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1622+104G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133768268 | ||||||
chr3:133768620
|
T | TGAGTG | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(182): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1622+460_1622+464d others(7): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 133768620 | |||||
chr3:133768650
|
T | C | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622+486T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133768650 | ||||||
chr3:133768777
|
C | G | 68 | a0001c0005t0012g0023a0001c0005t0012g0153a0001c0005t0012g0166others(65): Show | 69 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1622+613C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133768777 | ||||||
chr3:133768784
|
A | AT | 32 | a0001c0003t0023g0025a0001c0003t0039g0223a0001c0003t0049g0218others(29): Show | 34 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1622+645dupT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 133768784 | |||||
chr3:133768784
|
AT | A | 29 | a0001c0001t0001g0079a0001c0001t0008g0064a0001c0001t0054g0038others(26): Show | 31 | HG00558.hp1 HG01070.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1622+645delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 133768784 | |||||
chr3:133768784
|
ATT | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 121 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1622+644_1622+645d others(4): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 133768784 | |||||
chr3:133768784
|
ATTT | A | 61 | a0001c0003t0124g0156a0001c0003t0224g0217a0001c0005t0012g0023others(58): Show | 63 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1622+643_1622+645d others(5): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 133768784 | |||||
chr3:133768963
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1622+799T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133768963 | ||||||
chr3:133769223
|
T | A | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1622+1059T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133769223 | ||||||
chr3:133769413
|
A | C | 2 | a0001c0004t0004g0203a0001c0004t0019g0205 | 2 | NA19057.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1623-1095A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133769413 | ||||||
chr3:133769727
|
C | T | 1 | a0001c0003t0123g0115 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1623-781C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133769727 | ||||||
chr3:133769826
|
T | C | 5 | a0002c0002t0014g0130a0002c0002t0014g0132a0002c0002t0014g0150others(2): Show | 5 | HG00621.hp2 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623-682T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133769826 | ||||||
chr3:133770033
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(182): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1623-475A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133770033 | ||||||
chr3:133770197
|
T | C | 2 | a0001c0004t0004g0203a0001c0004t0019g0205 | 2 | NA19057.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1623-311T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133770197 | ||||||
chr3:133770199
|
G | A | 5 | a0001c0003t0010g0006a0001c0003t0118g0006a0004c0010t0010g0006others(2): Show | 7 | NA18962.hp2 NA19062.hp1 NA19064.hp1 others(4): Show |
intron_variant | MODIFIER | c.1623-309G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133770199 | ||||||
chr3:133770444
|
CT | C | 3 | a0001c0003t0023g0025a0001c0003t0181g0025a0008c0023t0023g0228 | 4 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623-63delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 13/16 | chr3 | 133770444 | ||||||
chr3:133770738
|
C | T | 1 | a0002c0002t0177g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1687+166C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133770738 | ||||||
chr3:133770739
|
G | A | 47 | a0001c0003t0023g0025a0001c0003t0181g0025a0001c0005t0012g0023others(44): Show | 48 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1687+167G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133770739 | ||||||
chr3:133771189
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1687+617A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771189 | ||||||
chr3:133771463
|
C | T | 1 | a0001c0004t0164g0201 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1687+891C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771463 | ||||||
chr3:133771466
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1687+894A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771466 | ||||||
chr3:133771476
|
G | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0092a0001c0001t0006g0012others(4): Show | 11 | HG01255.hp1 HG01943.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1687+904G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771476 | ||||||
chr3:133771490
|
A | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(273): Show | 307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1687+918A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771490 | ||||||
chr3:133771579
|
T | C | 1 | a0001c0003t0057g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1687+1007T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771579 | ||||||
chr3:133771609
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0002g0005others(5): Show | 12 | HG00544.hp2 HG02523.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.1687+1037C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771609 | ||||||
chr3:133771661
|
T | C | 54 | a0001c0003t0023g0025a0001c0003t0181g0025a0001c0005t0012g0023others(51): Show | 57 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1687+1089T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771661 | ||||||
chr3:133771669
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1687+1097G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771669 | ||||||
chr3:133771714
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1687+1142G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771714 | ||||||
chr3:133771739
|
G | A | 1 | a0001c0006t0140g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1687+1167G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771739 | ||||||
chr3:133771743
|
C | CA | 58 | a0001c0003t0023g0025a0001c0003t0034g0114a0001c0003t0048g0220others(55): Show | 59 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1687+1194dupA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAA | 25 | a0001c0003t0070g0121a0001c0003t0138g0125a0001c0003t0148g0108others(22): Show | 26 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1687+1189_1687+119 others(10): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(5): Show |
1 | a0001c0003t0122g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1687+1183_1687+119 others(16): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(9): Show |
18 | a0001c0006t0044g0048a0001c0006t0045g0030a0001c0006t0046g0180others(15): Show | 24 | HG00544.hp1 HG01081.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1687+1179_1687+119 others(20): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(10): Show |
33 | a0001c0006t0044g0229a0001c0006t0046g0179a0001c0006t0140g0178others(30): Show | 35 | HG00609.hp1 HG00621.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1687+1178_1687+119 others(21): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(11): Show |
11 | a0001c0006t0111g0151a0001c0006t0186g0060a0001c0006t0187g0058others(8): Show | 11 | HG01123.hp2 HG02015.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1687+1177_1687+119 others(22): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(12): Show |
1 | a0001c0003t0112g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1687+1176_1687+119 others(23): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(13): Show |
1 | a0002c0002t0107g0149 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1687+1175_1687+119 others(24): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(14): Show |
1 | a0001c0006t0191g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1687+1174_1687+119 others(25): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(17): Show |
2 | a0005c0011t0021g0018a0005c0011t0022g0018 | 3 | HG02922.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1687+1194_1687+119 others(28): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
C | CAAAAAAA others(18): Show |
1 | a0005c0011t0022g0028 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1687+1194_1687+119 others(29): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
CA | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0232a0001c0001t0052g0076others(4): Show | 7 | HG01106.hp1 HG02080.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1687+1194delA | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771743
|
CAA | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 124 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1687+1193_1687+119 others(6): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133771743 | |||||
chr3:133771768
|
A | G | 2 | a0001c0003t0147g0241a0001c0003t0237g0240 | 2 | HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1687+1196A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771768 | ||||||
chr3:133771777
|
G | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(111): Show | 133 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1687+1205G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133771777 | ||||||
chr3:133772193
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1687+1621G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772193 | ||||||
chr3:133772493
|
T | C | 13 | a0001c0005t0073g0158a0001c0007t0017g0019a0001c0007t0017g0035others(10): Show | 13 | HG02895.hp2 HG02970.hp1 HG04204.hp1 others(10): Show |
intron_variant | MODIFIER | c.1687+1921T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772493 | ||||||
chr3:133772501
|
G | T | 1 | a0006c0013t0144g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1687+1929G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772501 | ||||||
chr3:133772601
|
C | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0066others(64): Show | 80 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.1687+2029C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772601 | ||||||
chr3:133772662
|
C | T | 1 | a0001c0006t0111g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1687+2090C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772662 | ||||||
chr3:133772726
|
TGAAATA | T | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(303): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.1687+2155_1687+216 others(10): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772726 | ||||||
chr3:133772846
|
T | C | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1687+2274T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772846 | ||||||
chr3:133772915
|
C | T | 1 | a0001c0004t0035g0200 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1687+2343C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133772915 | ||||||
chr3:133773149
|
C | T | 1 | a0001c0017t0028g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1688-2284C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773149 | ||||||
chr3:133773244
|
A | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1688-2189A>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773244 | ||||||
chr3:133773266
|
G | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-2167G>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773266 | ||||||
chr3:133773352
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1688-2081G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773352 | ||||||
chr3:133773451
|
C | T | 3 | a0001c0004t0004g0199a0001c0004t0160g0198a0001c0004t0166g0196 | 3 | NA18949.hp2 NA19007.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1688-1982C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773451 | ||||||
chr3:133773452
|
G | A | 3 | a0001c0001t0252g0027a0001c0001t0253g0027a0001c0003t0056g0051 | 4 | HG01496.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1688-1981G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773452 | ||||||
chr3:133773453
|
C | T | 1 | a0001c0005t0069g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1688-1980C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773453 | ||||||
chr3:133773485
|
T | TTG | 49 | a0001c0001t0025g0032a0001c0001t0049g0103a0001c0003t0010g0006others(46): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1688-1918_1688-191 others(6): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773485
|
T | TTGTG | 37 | a0001c0003t0122g0171a0001c0003t0150g0097a0001c0005t0012g0023others(34): Show | 37 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1688-1920_1688-191 others(8): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773485
|
T | TTGTGTG | 3 | a0001c0005t0012g0153a0001c0005t0061g0161a0001c0005t0062g0164 | 3 | HG02622.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1688-1922_1688-191 others(10): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773485
|
T | TTGTGTGT others(1): Show |
3 | a0001c0005t0063g0155a0001c0005t0065g0154a0001c0005t0080g0162 | 3 | HG02055.hp1 HG02818.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1688-1924_1688-191 others(12): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773485
|
TTG | T | 35 | a0001c0004t0040g0193a0002c0002t0003g0136a0002c0002t0015g0008others(32): Show | 37 | HG00609.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1688-1918_1688-191 others(6): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773485
|
TTGTG | T | 34 | a0001c0001t0001g0078a0001c0001t0216g0105a0001c0001t0261g0068others(31): Show | 39 | HG00544.hp1 HG00621.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1688-1920_1688-191 others(8): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773485
|
TTGTGTG | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1688-1922_1688-191 others(10): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133773485 | |||||
chr3:133773487
|
G | C | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1688-1946G>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773487 | ||||||
chr3:133773578
|
G | A | 1 | a0001c0001t0006g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1688-1855G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773578 | ||||||
chr3:133773627
|
G | A | 32 | a0001c0001t0025g0032a0001c0001t0049g0103a0001c0003t0010g0006others(29): Show | 37 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1688-1806G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773627 | ||||||
chr3:133773657
|
G | A | 2 | a0001c0004t0160g0198a0001c0004t0166g0196 | 2 | NA18949.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1688-1776G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773657 | ||||||
chr3:133773809
|
A | G | 1 | a0001c0001t0057g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1688-1624A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773809 | ||||||
chr3:133773911
|
C | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-1522C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133773911 | ||||||
chr3:133774051
|
C | T | 6 | a0001c0007t0017g0019a0001c0007t0017g0035a0001c0007t0037g0035others(3): Show | 6 | NA18951.hp1 NA18953.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1688-1382C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133774051 | ||||||
chr3:133774194
|
T | A | 1 | a0001c0001t0054g0038 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1688-1239T>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133774194 | ||||||
chr3:133774485
|
TAC | T | 3 | a0005c0011t0021g0018a0005c0011t0022g0018a0005c0011t0022g0028 | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-946_1688-945d others(4): Show |
TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133774485 | |||||
chr3:133774861
|
GT | G | 344 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(341): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1688-558delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr3 | 133774861 | |||||
chr3:133774864
|
T | G | 2 | a0001c0003t0023g0025a0001c0003t0181g0025 | 3 | HG01109.hp1 HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1688-569T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133774864 | ||||||
chr3:133774865
|
T | G | 1 | a0008c0023t0023g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1688-568T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133774865 | ||||||
chr3:133774983
|
T | C | 51 | a0001c0003t0023g0025a0001c0003t0181g0025a0001c0005t0012g0023others(48): Show | 52 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1688-450T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133774983 | ||||||
chr3:133775236
|
C | T | 1 | a0001c0004t0159g0192 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1688-197C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133775236 | ||||||
chr3:133775331
|
G | A | 3 | a0001c0001t0261g0068a0001c0001t0262g0069a0001c0003t0127g0152 | 3 | HG02055.hp2 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1688-102G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133775331 | ||||||
chr3:133775381
|
C | T | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1688-52C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133775381 | ||||||
chr3:133775394
|
C | A | 4 | a0001c0014t0059g0237a0001c0014t0059g0238a0001c0015t0267g0182others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1688-39C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133775394 | ||||||
chr3:133775429
|
C | A | 1 | a0001c0003t0007g0043 | 2 | HG00642.hp2 HG01192.hp1 |
splice_region_variant&intron_variant | LOW | c.1688-4C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 14/16 | chr3 | 133775429 | ||||||
chr3:133775685
|
C | A | 20 | a0001c0005t0028g0165a0001c0005t0029g0044a0001c0005t0029g0170others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1872+68C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133775685 | ||||||
chr3:133776005
|
T | C | 55 | a0001c0003t0023g0025a0001c0003t0138g0125a0001c0003t0181g0025others(52): Show | 58 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1872+388T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776005 | ||||||
chr3:133776115
|
C | T | 5 | a0001c0003t0138g0125a0001c0014t0059g0237a0001c0014t0059g0238others(2): Show | 5 | HG02647.hp2 HG02896.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1872+498C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776115 | ||||||
chr3:133776173
|
T | C | 52 | a0001c0003t0023g0025a0001c0003t0138g0125a0001c0003t0181g0025others(49): Show | 53 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1872+556T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776173 | ||||||
chr3:133776218
|
G | A | 4 | a0001c0003t0070g0121a0001c0003t0148g0108a0001c0006t0149g0089others(1): Show | 4 | HG01243.hp2 HG02559.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1872+601G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776218 | ||||||
chr3:133776441
|
A | T | 5 | a0002c0002t0099g0134a0002c0002t0102g0139a0005c0011t0021g0018others(2): Show | 7 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1873-608A>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776441 | ||||||
chr3:133776539
|
T | G | 13 | a0001c0006t0044g0048a0001c0006t0044g0229a0001c0006t0045g0030others(10): Show | 14 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1873-510T>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776539 | ||||||
chr3:133776617
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1873-432A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776617 | ||||||
chr3:133776768
|
G | A | 1 | a0001c0001t0006g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1873-281G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776768 | ||||||
chr3:133776818
|
G | A | 1 | a0001c0004t0172g0211 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1873-231G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776818 | ||||||
chr3:133776829
|
C | A | 44 | a0001c0005t0012g0023a0001c0005t0012g0153a0001c0005t0012g0166others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1873-220C>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776829 | ||||||
chr3:133776838
|
C | G | 2 | a0001c0003t0224g0217a0001c0003t0265g0216 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1873-211C>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 15/16 | chr3 | 133776838 | ||||||
chr3:133777709
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 131 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.2062+471T>C | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 16/16 | chr3 | 133777709 | ||||||
chr3:133777782
|
A | G | 1 | a0001c0001t0026g0253 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2062+544A>G | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 16/16 | chr3 | 133777782 | ||||||
chr3:133778079
|
C | T | 1 | a0002c0002t0174g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2063-507C>T | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 16/16 | chr3 | 133778079 | ||||||
chr3:133778080
|
G | A | 1 | a0002c0002t0104g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2063-506G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 16/16 | chr3 | 133778080 | ||||||
chr3:133778166
|
G | A | 1 | a0001c0003t0025g0221 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2063-420G>A | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 16/16 | chr3 | 133778166 | ||||||
chr3:133778421
|
GT | G | 6 | a0001c0005t0012g0153a0001c0005t0012g0166a0001c0005t0027g0163others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2063-164delT | TF | ENSG00000091513.16 | transcript | ENST00000402696.9 | protein_coding | 16/16 | chr3 | 133778421 |