Item | Value |
---|---|
geneid | 4922 |
ensemblid | ENSG00000133636.11 |
hgncid | 8038 |
symbol | NTS |
name | neurotensin |
refseq_nuc | NM_006183.5 |
refseq_prot | NP_006174.1 |
ensembl_nuc | ENST00000256010.7 |
ensembl_prot | ENSP00000256010.5 |
mane_status | MANE Select |
chr | chr12 |
start | 85874295 |
end | 85882992 |
strand | + |
ver | v1.2 |
region | chr12:85874295-85882992 |
region5000 | chr12:85869295-85887992 |
regionname0 | NTS_chr12_85874295_85882992 |
regionname5000 | NTS_chr12_85869295_85887992 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 170 | 417 | 91 | 79 | 183 | 16 | 46 | 141 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0002 | 0/0 | 170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0003 | 0/0 | 170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0004 | 0/0 | 170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 513 | 416 | 90 | 79 | 183 | 16 | 46 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
c0002 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
c0003 | 0/0 | 513 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
c0004 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
c0005 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 727 | 364 | 86 | 73 | 146 | 14 | 43 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0002 | 0/0 | 727 | 41 | 0 | 3 | 35 | 0 | 3 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0003 | 0/0 | 723 | 5 | 0 | 3 | 0 | 2 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0004 | 0/0 | 727 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0005 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0006 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0007 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0008 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0009 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0010 | 0/0 | 727 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
t0011 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 69 | 7 | 8 | 49 | 2 | 3 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0002 | 0/0 | 42 | 0 | 14 | 19 | 1 | 8 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0003 | 0/0 | 12 | 1 | 10 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0004 | 0/1 | 11 | 0 | 6 | 0 | 2 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0007 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0008 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0009 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0010 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0021 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0042 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0046 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 513 | 416 | 90 | 79 | 183 | 16 | 46 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
a0001c0004 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
a0002c0003 | 0/0 | 513 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
a0003c0002 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 | |
a0004c0005 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1239 | 362 | 85 | 72 | 146 | 14 | 43 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0002 | 0/0 | 1239 | 40 | 0 | 3 | 34 | 0 | 3 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0003 | 0/0 | 1235 | 5 | 0 | 3 | 0 | 2 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0004 | 0/0 | 1239 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0005 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0006 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0008 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0009 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0010 | 0/0 | 1239 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0001t0011 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0001c0004t0001 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0002c0003t0001 | 0/0 | 1239 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0003c0002t0007 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
a0004c0005t0002 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | copy fasta | chr12 | 85869295 | 85887992 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 66 | 6 | 8 | 47 | 2 | 3 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0002 | 0/0 | 42 | 0 | 14 | 19 | 1 | 8 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0003 | 0/0 | 12 | 1 | 10 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0004 | 0/1 | 11 | 0 | 6 | 0 | 2 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0010 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0042 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0007 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0004g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0002c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0003c0002t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
a0004c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00423 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0115 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01978 | hp1 | a0002 | c0003 | t0001 | g0132 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02922 | hp2 | a0001 | c0001 | t0011 | g0176 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19091 | hp2 | a0004 | c0005 | t0002 | g0079 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0138 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
NA21309 | hp2 | a0003 | c0002 | t0007 | g0001 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:85874446 | C | G | 1 | a0004 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.43C>G | p.Leu15Val | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/4 | 152/1239 | 43/513 | 15/170 | chr12 | 85874446 | ||
chr12:85876677 | C | A | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.111C>A | p.Phe37Leu | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/4 | 220/1239 | 111/513 | 37/170 | chr12 | 85876677 | ||
chr12:85878399 | C | A | 1 | a0002 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.190C>A | p.Leu64Ile | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/4 | 299/1239 | 190/513 | 64/170 | chr12 | 85878399 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:85882366 | C | T | 1 | a0001c0004 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.504C>T | p.Tyr168Tyr | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 613/1239 | 504/513 | 168/170 | chr12 | 85882366 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:85874401 | A | G | 3 | a0001c0001t0003a0001c0001t0010a0001c0001t0011 | 7 | HG00639.hp2 HG00741.hp2 HG01175.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-3A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/4 | 3 | chr12 | 85874401 | |||||
chr12:85882507 | T | A | 1 | a0001c0001t0005 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 132 | chr12 | 85882507 | |||||
chr12:85882518 | A | G | 1 | a0001c0001t0009 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*143A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 143 | chr12 | 85882518 | |||||
chr12:85882569 | G | A | 3 | a0001c0001t0002a0001c0001t0010a0004c0005t0002 | 42 | HG01175.hp1 HG01928.hp2 HG01952.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*194G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 194 | chr12 | 85882569 | |||||
chr12:85882691 | G | A | 1 | a0001c0001t0006 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 316 | chr12 | 85882691 | |||||
chr12:85882707 | C | T | 1 | a0001c0001t0008 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 332 | chr12 | 85882707 | |||||
chr12:85882802 | G | A | 1 | a0003c0002t0007 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 427 | chr12 | 85882802 | |||||
chr12:85882875 | AGATT | A | 1 | a0001c0001t0003 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*505_*508delGATT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 505 | INFO_REALIGN_3_PRIME | chr12 | 85882875 | ||||
chr12:85882909 | T | A | 1 | a0001c0001t0004 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*534T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 534 | chr12 | 85882909 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:85874633 | C | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73+157C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874633 | ||||||
chr12:85874705 | C | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.73+229C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874705 | ||||||
chr12:85874881 | G | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+405G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874881 | ||||||
chr12:85874896 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.73+420C>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874896 | ||||||
chr12:85875060 | C | T | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 6 | HG02055.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+584C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875060 | ||||||
chr12:85875163 | T | G | 4 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057others(1): Show | 6 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+687T>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875163 | ||||||
chr12:85875217 | G | A | 4 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057others(1): Show | 6 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+741G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875217 | ||||||
chr12:85875224 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.73+748C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875224 | ||||||
chr12:85875268 | C | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 7 | HG02109.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+792C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875268 | ||||||
chr12:85875391 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.73+915G>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875391 | ||||||
chr12:85875662 | A | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 6 | NA18954.hp2 NA18973.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.74-978A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875662 | ||||||
chr12:85875692 | T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.74-948T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875692 | ||||||
chr12:85876074 | G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.74-566G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876074 | ||||||
chr12:85876106 | C | CA | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.74-532dupA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 85876106 | |||||
chr12:85876140 | AC | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 7 | HG01192.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-499delC | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876140 | ||||||
chr12:85876173 | T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-467T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876173 | ||||||
chr12:85876231 | T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-409T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876231 | ||||||
chr12:85876244 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.74-396A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876244 | ||||||
chr12:85876271 | A | G | 1 | a0001c0001t0001g0022 | 3 | NA18990.hp1 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.74-369A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876271 | ||||||
chr12:85876405 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.74-235T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876405 | ||||||
chr12:85876469 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.74-171A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876469 | ||||||
chr12:85876722 | A | G | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+21A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85876722 | ||||||
chr12:85876831 | G | GA | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.135+140dupA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85876831 | |||||
chr12:85876851 | GT | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.135+152delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85876851 | |||||
chr12:85877031 | T | A | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+330T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877031 | ||||||
chr12:85877053 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.135+352C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877053 | ||||||
chr12:85877072 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+371G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877072 | ||||||
chr12:85877077 | T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.135+376T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877077 | ||||||
chr12:85877272 | G | A | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+571G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877272 | ||||||
chr12:85877285 | G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.135+584G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877285 | ||||||
chr12:85877311 | A | T | 1 | a0001c0004t0001g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135+610A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877311 | ||||||
chr12:85877336 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.135+635T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877336 | ||||||
chr12:85877401 | CT | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.135+717delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85877401 | |||||
chr12:85877401 | CTT | C | 7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(4): Show | 8 | HG02055.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+716_135+717del others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85877401 | |||||
chr12:85877688 | G | A | 1 | a0001c0001t0004g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-657G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877688 | ||||||
chr12:85877719 | A | G | 2 | a0001c0001t0004g0049a0001c0001t0004g0146 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.136-626A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877719 | ||||||
chr12:85877781 | G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG00621.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.136-564G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877781 | ||||||
chr12:85877796 | A | T | 1 | a0001c0001t0001g0055 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.136-549A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877796 | ||||||
chr12:85877891 | T | TAACAATT others(25): Show |
1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136-453_136-422dup others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85877891 | |||||
chr12:85878038 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-307T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878038 | ||||||
chr12:85878124 | C | T | 2 | a0001c0001t0004g0049a0001c0001t0004g0146 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.136-221C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878124 | ||||||
chr12:85878133 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.136-212G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878133 | ||||||
chr12:85878325 | G | T | 1 | a0001c0001t0003g0057 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.136-20G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878325 | ||||||
chr12:85878573 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02922.hp1 | splice_region_variant&intron_variant | LOW | c.360+4T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85878573 | ||||||
chr12:85878600 | A | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.360+31A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85878600 | ||||||
chr12:85878795 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.360+226T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85878795 | ||||||
chr12:85879036 | T | TTTTATGT others(24): Show |
1 | a0001c0001t0001g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360+475_360+476ins others(31): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879036 | |||||
chr12:85879039 | T | TATGTATA others(5): Show |
3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+475_360+476ins others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879039 | |||||
chr12:85879045 | C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.360+476C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879045 | ||||||
chr12:85879071 | TA | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0080a0001c0001t0001g0124others(2): Show | 6 | HG02132.hp2 NA18947.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+504delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879071 | |||||
chr12:85879079 | A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0080others(4): Show | 10 | HG01168.hp1 HG02132.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.360+510A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879079 | ||||||
chr12:85879089 | T | TTTTTATG others(151): Show |
1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+536_360+537ins others(158): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879089 | |||||
chr12:85879089 | T | TTTTTATG others(363): Show |
1 | a0001c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.360+540_360+541ins others(370): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879089 | |||||
chr12:85879098 | A | ATGTACGT others(49): Show |
1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+530_360+531ins others(56): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879098 | |||||
chr12:85879100 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.360+531A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879100 | ||||||
chr12:85879110 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.360+541C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879110 | ||||||
chr12:85879111 | G | A | 4 | a0001c0001t0001g0013a0001c0001t0003g0016a0001c0001t0003g0056others(1): Show | 9 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+542G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879111 | ||||||
chr12:85879121 | T | TTTTATGT others(54): Show |
1 | a0001c0001t0001g0124 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.360+555_360+556ins others(61): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879121 | |||||
chr12:85879121 | T | TTTTTATG others(55): Show |
3 | a0001c0001t0001g0147a0001c0001t0004g0049a0001c0001t0004g0146 | 4 | HG02055.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+587_360+588ins others(62): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879121 | |||||
chr12:85879143 | G | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+574G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879143 | ||||||
chr12:85879152 | AT | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 8 | HG03130.hp1 HG03139.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+588delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879152 | |||||
chr12:85879153 | T | TTTTATGT others(85): Show |
2 | a0001c0001t0001g0126a0001c0001t0001g0141 | 2 | HG02132.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.360+587_360+588ins others(92): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879153 | T | TTTTATGT others(147): Show |
1 | a0001c0001t0001g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.360+587_360+588ins others(154): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879153 | T | TTTTTATG others(86): Show |
1 | a0001c0001t0002g0061 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+605_360+606ins others(93): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879153 | T | TTTTTATG others(106): Show |
1 | a0001c0001t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.360+619_360+620ins others(113): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879153 | T | TTTTTATG others(117): Show |
1 | a0001c0001t0001g0085 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.360+619_360+620ins others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879153 | T | TTTTTATG others(117): Show |
1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.360+619_360+620ins others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879153 | T | TTTTTATG others(97): Show |
1 | a0001c0001t0001g0013 | 4 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+619_360+620ins others(104): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | |||||
chr12:85879156 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.360+587T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879156 | ||||||
chr12:85879160 | G | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0161a0001c0001t0004g0049others(1): Show | 5 | HG02055.hp1 HG02630.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+591G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879160 | ||||||
chr12:85879162 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.360+593A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879162 | ||||||
chr12:85879163 | T | TATTTTAT others(4): Show |
3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+595_360+605dup others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879163 | |||||
chr12:85879174 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.360+605C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879174 | ||||||
chr12:85879175 | G | A | 4 | a0001c0001t0001g0161a0001c0001t0003g0016a0001c0001t0003g0056others(1): Show | 6 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+606G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879175 | ||||||
chr12:85879184 | AT | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(110): Show | 293 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.360+620delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879184 | |||||
chr12:85879185 | T | TTTTATGT others(54): Show |
1 | a0001c0001t0002g0033 | 2 | NA19058.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.360+619_360+620ins others(61): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879185 | |||||
chr12:85879185 | T | TTTTATGT others(116): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0074 | 3 | NA19005.hp1 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.360+619_360+620ins others(123): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879185 | |||||
chr12:85879188 | T | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0161 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.360+619T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879188 | ||||||
chr12:85879192 | G | A | 15 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(12): Show | 19 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.360+623G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879192 | ||||||
chr12:85879195 | T | TATTTTAT others(4): Show |
1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+627_360+637dup others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879195 | |||||
chr12:85879206 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.360+637C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879206 | ||||||
chr12:85879206 | CGTAAAAT others(13): Show |
C | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+638_360+657del others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879206 | ||||||
chr12:85879207 | G | A | 2 | a0001c0001t0001g0156a0001c0001t0003g0056 | 2 | HG00639.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.360+638G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879207 | ||||||
chr12:85879216 | A | AT | 27 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(24): Show | 55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.360+649dupT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(139): Show |
1 | a0001c0001t0002g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.360+649_360+650ins others(146): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(88): Show |
1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+649_360+650ins others(95): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(181): Show |
1 | a0001c0001t0001g0035 | 2 | HG00738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.360+649_360+650ins others(188): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(150): Show |
13 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0046others(10): Show | 22 | HG01175.hp2 HG01928.hp1 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(150): Show |
1 | a0001c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.360+649_360+650ins others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(119): Show |
41 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(38): Show | 128 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(126): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(88): Show |
11 | a0001c0001t0001g0045a0001c0001t0001g0112a0001c0001t0001g0113others(8): Show | 21 | HG01175.hp1 HG01928.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(95): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(120): Show |
1 | a0001c0001t0002g0107 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.360+649_360+650ins others(127): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(130): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0071 | 8 | HG00140.hp2 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(137): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(99): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(9): Show | 59 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(106): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTATG others(131): Show |
1 | a0001c0001t0001g0017 | 3 | HG01069.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.360+649_360+650ins others(138): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTTAT others(150): Show |
4 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0134others(1): Show | 7 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTTAT others(120): Show |
1 | a0001c0001t0001g0173 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.360+649_360+650ins others(127): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879216 | A | ATTTTTAT others(182): Show |
1 | a0001c0001t0001g0135 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.360+649_360+650ins others(189): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | |||||
chr12:85879217 | T | TTTTATGT others(121): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0174 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+649_360+650ins others(128): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879217 | |||||
chr12:85879219 | A | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.360+650A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879219 | ||||||
chr12:85879223 | A | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.360+654A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879223 | ||||||
chr12:85879237 | T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.360+668T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879237 | ||||||
chr12:85879238 | G | A | 3 | a0001c0001t0001g0161a0001c0001t0003g0016a0001c0001t0003g0057 | 5 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+669G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879238 | ||||||
chr12:85879238 | G | T | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+669G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879238 | ||||||
chr12:85879240 | A | T | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+671A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879240 | ||||||
chr12:85879241 | A | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0156 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+672A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879241 | ||||||
chr12:85879242 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+673_360+674ins others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879242 | ||||||
chr12:85879242 | A | T | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+673A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879242 | ||||||
chr12:85879243 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+674A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879243 | ||||||
chr12:85879243 | A | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0156 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+674A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879243 | ||||||
chr12:85879245 | A | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0156 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+676A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879245 | ||||||
chr12:85879246 | TATTATAC others(3): Show |
T | 2 | a0001c0001t0001g0120a0001c0001t0001g0161 | 2 | HG03471.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.360+681_360+690del others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879246 | |||||
chr12:85879247 | A | AT | 16 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0047others(13): Show | 20 | HG01081.hp1 HG01175.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.360+680dupT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879247 | |||||
chr12:85879247 | A | ATTT | 7 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0148others(4): Show | 13 | HG00639.hp1 HG01884.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+680_360+681ins others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879247 | |||||
chr12:85879248 | T | TTTA | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(90): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.360+680_360+681ins others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879248 | |||||
chr12:85879248 | TTATACAT others(2): Show |
T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+681_360+689del others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879248 | |||||
chr12:85879249 | T | A | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+680T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879249 | ||||||
chr12:85879249 | T | TTTATGTA others(46): Show |
1 | a0001c0001t0001g0043 | 2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+680_360+681ins others(53): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879249 | ||||||
chr12:85879249 | T | TTTTATAT others(16): Show |
1 | a0001c0001t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360+680_360+681ins others(23): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879249 | ||||||
chr12:85879250 | A | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.360+681A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879250 | ||||||
chr12:85879251 | T | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0166a0001c0001t0003g0056 | 4 | HG00639.hp2 HG02135.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+682T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879251 | ||||||
chr12:85879253 | C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.360+684C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879253 | ||||||
chr12:85879254 | A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.360+685A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879254 | ||||||
chr12:85879255 | T | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0156 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+686T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879255 | ||||||
chr12:85879256 | A | AT | 41 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(1): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(161): Show |
1 | a0001c0001t0001g0034 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.360+687_360+688ins others(168): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(307): Show |
1 | a0001c0001t0001g0048 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+687_360+688ins others(314): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(205): Show |
1 | a0001c0001t0001g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(212): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(205): Show |
1 | a0001c0001t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(212): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(100): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0038 | 8 | HG02280.hp1 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(107): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(183): Show |
1 | a0001c0001t0001g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(190): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(163): Show |
4 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0080others(1): Show | 6 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(170): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(229): Show |
1 | a0001c0001t0001g0162 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(236): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(163): Show |
1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(170): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(103): Show |
1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(110): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(100): Show |
1 | a0001c0001t0002g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(107): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(101): Show |
3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | NA18940.hp1 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.360+687_360+688ins others(108): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(100): Show |
1 | a0001c0001t0002g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(107): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(132): Show |
4 | a0001c0001t0002g0006a0001c0001t0002g0110a0001c0001t0002g0111others(1): Show | 13 | HG02015.hp1 HG02135.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(139): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(135): Show |
1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(142): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(166): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0169 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.360+687_360+688ins others(173): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(197): Show |
3 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0158 | 4 | HG02559.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(204): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATATTTTA others(36): Show |
2 | a0001c0001t0001g0067a0001c0001t0002g0086 | 2 | HG03704.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.360+687_360+688ins others(43): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATTTTATG others(67): Show |
1 | a0001c0001t0001g0148 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(74): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATTTTATG others(101): Show |
1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(108): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATTTTATG others(112): Show |
1 | a0001c0001t0001g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(119): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATTTTATG others(132): Show |
4 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0159others(1): Show | 10 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(139): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879256 | A | ATTTTATG others(3): Show |
90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(87): Show | 257 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | ||||||
chr12:85879257 | A | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0166a0001c0001t0003g0056 | 4 | HG00639.hp2 HG02135.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+688A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879257 | ||||||
chr12:85879264 | G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0166 | 3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+695G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879264 | ||||||
chr12:85879264 | G | GTACGTAA others(2): Show |
13 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0052others(10): Show | 37 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.360+697_360+698ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | |||||
chr12:85879264 | G | GTACGTAA others(67): Show |
1 | a0001c0001t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.360+697_360+698ins others(74): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | |||||
chr12:85879264 | G | GTACGTAA others(68): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0152others(1): Show | 16 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.360+697_360+698ins others(75): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | |||||
chr12:85879264 | G | GTACGTAA others(80): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0154 | 7 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+697_360+698ins others(87): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | |||||
chr12:85879264 | G | GTACGTAA others(66): Show |
1 | a0001c0001t0002g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.360+697_360+698ins others(73): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | |||||
chr12:85879266 | A | ACGTAAAA others(136): Show |
1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+697_360+698ins others(143): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879266 | ||||||
chr12:85879267 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+698T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879267 | ||||||
chr12:85879268 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.360+699A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879268 | ||||||
chr12:85879269 | T | TAAAA | 2 | a0001c0001t0001g0050a0001c0001t0001g0174 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+700_360+701ins others(4): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879269 | ||||||
chr12:85879271 | T | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0174 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+702T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879271 | ||||||
chr12:85879271 | T | TA | 6 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0152others(3): Show | 18 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.360+702_360+703ins others(1): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879271 | ||||||
chr12:85879275 | G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0141others(6): Show | 21 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.360+706G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879275 | ||||||
chr12:85879275 | G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0174 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+706G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879275 | ||||||
chr12:85879278 | T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0120a0001c0001t0001g0166 | 4 | HG02135.hp1 HG02572.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+709T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879278 | ||||||
chr12:85879279 | A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0120a0001c0001t0001g0166 | 4 | HG02135.hp1 HG02572.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+710A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879279 | ||||||
chr12:85879280 | T | TTTTATGT others(82): Show |
1 | a0001c0001t0001g0172 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.360+711_360+712ins others(89): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879280 | ||||||
chr12:85879280 | TACC | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0174 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+713_360+715del others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879280 | |||||
chr12:85879281 | A | ATTTT | 3 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0173 | 3 | HG02071.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+712_360+713ins others(4): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879281 | ||||||
chr12:85879281 | A | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(19): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.360+712A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879281 | ||||||
chr12:85879282 | C | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(152): Show | 353 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.360+713C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879282 | ||||||
chr12:85879282 | C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(18): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.360+713C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879282 | ||||||
chr12:85879283 | C | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(148): Show | 349 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.360+714C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879283 | ||||||
chr12:85879283 | C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(22): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.360+714C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879283 | ||||||
chr12:85879284 | A | ATG | 9 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 25 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.360+716_360+717ins others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | |||||
chr12:85879284 | A | ATGTACGT others(61): Show |
1 | a0001c0001t0001g0168 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.360+716_360+717ins others(68): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | |||||
chr12:85879284 | A | ATGTACGT others(122): Show |
1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.360+716_360+717ins others(129): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | |||||
chr12:85879284 | A | ATGTACGT others(93): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0052others(5): Show | 32 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.360+716_360+717ins others(100): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | |||||
chr12:85879284 | A | ATGTACGT others(91): Show |
1 | a0001c0001t0001g0103 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.360+716_360+717ins others(98): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | |||||
chr12:85879284 | A | ATGTACGT others(123): Show |
1 | a0001c0001t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.360+716_360+717ins others(130): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | |||||
chr12:85879284 | A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0173 | 3 | HG02071.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+715A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879284 | ||||||
chr12:85879295 | G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0166 | 3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+726G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879295 | ||||||
chr12:85879295 | G | GTATATAA others(2): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0151others(1): Show | 8 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+731_360+732ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879295 | |||||
chr12:85879303 | TATGTATA others(13): Show |
T | 1 | a0001c0001t0001g0172 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.360+743_360+762del others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879303 | |||||
chr12:85879309 | T | C | 2 | a0001c0001t0001g0120a0001c0001t0002g0060 | 2 | HG02148.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.360+740T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879309 | ||||||
chr12:85879310 | A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0120 | 3 | HG02135.hp1 NA18987.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.360+741A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879310 | ||||||
chr12:85879312 | A | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+743A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879312 | ||||||
chr12:85879313 | A | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+744A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879313 | ||||||
chr12:85879314 | A | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+745A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879314 | ||||||
chr12:85879315 | ATATATTT others(4): Show |
A | 3 | a0001c0001t0001g0090a0001c0001t0001g0118a0001c0001t0001g0148 | 3 | HG03453.hp2 HG03471.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.360+754_360+764del others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879315 | |||||
chr12:85879317 | A | G | 2 | a0001c0001t0001g0147a0001c0001t0011g0176 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.360+748A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879317 | ||||||
chr12:85879321 | T | A | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+752T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879321 | ||||||
chr12:85879323 | A | AT | 2 | a0001c0001t0001g0043a0001c0001t0001g0166 | 3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+754_360+755ins others(1): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879323 | ||||||
chr12:85879323 | A | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.360+754A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879323 | ||||||
chr12:85879325 | T | A | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+756T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879325 | ||||||
chr12:85879326 | G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0166a0001c0001t0011g0176 | 4 | HG02135.hp1 HG02572.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+757G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879326 | ||||||
chr12:85879326 | G | GTATATAA others(2): Show |
16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(13): Show | 52 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.360+762_360+763ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879326 | |||||
chr12:85879326 | G | GTATATTT others(13): Show |
2 | a0001c0001t0001g0149a0001c0001t0002g0109 | 2 | HG02074.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+773_360+774ins others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879326 | |||||
chr12:85879327 | T | C | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+758T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879327 | ||||||
chr12:85879331 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+762T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879331 | ||||||
chr12:85879332 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+763T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879332 | ||||||
chr12:85879337 | G | GTACGTAA others(78): Show |
1 | a0001c0001t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.360+770_360+771ins others(85): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879337 | |||||
chr12:85879337 | G | GTATATAA others(2): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0156a0001c0001t0001g0161others(1): Show | 4 | HG02572.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+773_360+774ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879337 | |||||
chr12:85879338 | T | TATATAAA others(2): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0154 | 7 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+773_360+774ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879338 | |||||
chr12:85879343 | T | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0157others(4): Show | 8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+774T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879343 | ||||||
chr12:85879344 | T | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0157others(4): Show | 8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+775T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879344 | ||||||
chr12:85879345 | T | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0157others(4): Show | 8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+776T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879345 | ||||||
chr12:85879348 | G | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0157others(4): Show | 8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+779G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879348 | ||||||
chr12:85879349 | TATATAAA others(2): Show |
T | 2 | a0001c0001t0001g0043a0001c0001t0001g0166 | 3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+785_360+793del others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879349 | |||||
chr12:85879351 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+782T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879351 | ||||||
chr12:85879352 | A | ATT | 6 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0120others(3): Show | 6 | HG02572.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+784_360+785ins others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879352 | |||||
chr12:85879352 | A | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0157others(4): Show | 8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+783A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879352 | ||||||
chr12:85879354 | A | T | 13 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 14 | HG00639.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+785A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879354 | ||||||
chr12:85879356 | A | T | 13 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 14 | HG00639.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+787A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879356 | ||||||
chr12:85879357 | A | ATATATTT others(4): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0154 | 7 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+788_360+789ins others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879357 | ||||||
chr12:85879357 | A | G | 13 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 14 | HG00639.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+788A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879357 | ||||||
chr12:85879358 | C | CATATTTT others(4): Show |
8 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0055others(5): Show | 15 | HG00639.hp1 HG00738.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.360+794_360+804dup others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879358 | |||||
chr12:85879358 | C | T | 19 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0051others(16): Show | 26 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.360+789C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879358 | ||||||
chr12:85879374 | A | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+805A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879374 | ||||||
chr12:85879375 | A | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+806A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879375 | ||||||
chr12:85879376 | A | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+807A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879376 | ||||||
chr12:85879378 | T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0156a0001c0001t0001g0161others(1): Show | 4 | HG02572.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+809T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879378 | ||||||
chr12:85879379 | A | G | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+810A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879379 | ||||||
chr12:85879381 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+812A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879381 | ||||||
chr12:85879381 | AT | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.360+817delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879381 | |||||
chr12:85879382 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+813T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879382 | ||||||
chr12:85879382 | T | TTTTATGT others(3): Show |
6 | a0001c0001t0001g0051a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 7 | HG02559.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+816_360+817ins others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879382 | |||||
chr12:85879384 | T | A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+815T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879384 | ||||||
chr12:85879386 | T | A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+817T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879386 | ||||||
chr12:85879386 | TA | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0089a0001c0001t0001g0120 | 4 | HG02135.hp1 HG02896.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+818delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879386 | ||||||
chr12:85879388 | T | A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+819T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879388 | ||||||
chr12:85879389 | G | A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+820G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879389 | ||||||
chr12:85879406 | A | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+837A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879406 | ||||||
chr12:85879407 | A | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+838A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879407 | ||||||
chr12:85879408 | A | T | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+839A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879408 | ||||||
chr12:85879409 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+849_360+860del others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879409 | |||||
chr12:85879410 | T | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0155a0001c0001t0001g0158others(1): Show | 5 | HG02559.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+841T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879410 | ||||||
chr12:85879411 | A | G | 1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+842A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879411 | ||||||
chr12:85879413 | AT | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.360+849delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879413 | |||||
chr12:85879414 | T | TTTTATGT others(14): Show |
1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.360+848_360+849ins others(21): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | |||||
chr12:85879414 | T | TTTTATGT others(25): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0048 | 4 | HG00738.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+848_360+849ins others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | |||||
chr12:85879414 | T | TTTTATGT others(87): Show |
1 | a0001c0001t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.360+848_360+849ins others(94): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | |||||
chr12:85879414 | T | TTTTATGT others(118): Show |
2 | a0001c0001t0001g0102a0001c0001t0008g0127 | 2 | HG02451.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.360+848_360+849ins others(125): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | |||||
chr12:85879418 | TA | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0089a0001c0001t0001g0120 | 4 | HG02135.hp1 HG02896.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+850delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879418 | ||||||
chr12:85879419 | A | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0102a0001c0001t0008g0127 | 3 | HG02451.hp2 HG03688.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.360+850A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879419 | ||||||
chr12:85879429 | T | A | 1 | a0001c0001t0001g0048 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+860T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879429 | ||||||
chr12:85879436 | A | ATT | 5 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+868_360+869ins others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879436 | |||||
chr12:85879438 | A | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+869A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879438 | ||||||
chr12:85879440 | A | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+871A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879440 | ||||||
chr12:85879441 | A | G | 5 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+872A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879441 | ||||||
chr12:85879450 | A | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0071others(6): Show | 11 | HG00738.hp2 HG02135.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.360+881A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879450 | ||||||
chr12:85879461 | A | ATGTATAT others(44): Show |
1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.360+899_360+900ins others(51): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879461 | |||||
chr12:85879463 | G | GTATATAA others(2): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(17): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.360+899_360+900ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | |||||
chr12:85879463 | G | GTATATAA others(33): Show |
1 | a0001c0001t0001g0170 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.360+899_360+900ins others(40): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | |||||
chr12:85879463 | G | GTATATAA others(95): Show |
2 | a0001c0001t0004g0049a0001c0001t0004g0146 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.360+899_360+900ins others(102): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | |||||
chr12:85879463 | G | GTATATTT others(13): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0174 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+910_360+911ins others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | |||||
chr12:85879467 | ATT | A | 8 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0071others(5): Show | 10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+901_360+902del others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879467 | |||||
chr12:85879471 | T | A | 8 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0071others(5): Show | 10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+902T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879471 | ||||||
chr12:85879472 | A | T | 4 | a0001c0001t0003g0016a0001c0001t0003g0057a0001c0001t0004g0049others(1): Show | 7 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+903A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879472 | ||||||
chr12:85879473 | T | A | 8 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0071others(5): Show | 10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+904T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879473 | ||||||
chr12:85879474 | G | A | 8 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0071others(5): Show | 10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+905G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879474 | ||||||
chr12:85879474 | G | GTATATAA others(2): Show |
21 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0027others(18): Show | 39 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.360+910_360+911ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | |||||
chr12:85879474 | G | GTATATAA others(33): Show |
1 | a0001c0001t0001g0048 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+910_360+911ins others(40): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | |||||
chr12:85879474 | G | GTATATAA others(95): Show |
1 | a0001c0001t0001g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.360+910_360+911ins others(102): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | |||||
chr12:85879474 | G | GTATATTT others(117): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0063others(1): Show | 8 | HG01361.hp1 HG02293.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+913_360+914ins others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | |||||
chr12:85879483 | A | ATGTATAT others(13): Show |
2 | a0001c0001t0004g0049a0001c0001t0004g0146 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.360+921_360+922ins others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(106): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0093others(1): Show | 4 | HG02735.hp1 HG03471.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+921_360+922ins others(113): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(168): Show |
1 | a0001c0001t0001g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.360+921_360+922ins others(175): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(24): Show |
2 | a0001c0001t0001g0101a0001c0001t0002g0116 | 2 | NA18612.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.360+995_360+1025du others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(116): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0112 | 3 | HG02622.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.360+976_360+977ins others(123): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(86): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0070a0001c0001t0001g0077others(2): Show | 9 | HG00408.hp1 HG01175.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.360+933_360+1025du others(94): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(117): Show |
67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(64): Show | 223 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(126): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(148): Show |
14 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0039others(11): Show | 25 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(179): Show |
1 | a0001c0001t0001g0024 | 3 | HG02257.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.360+1025_360+1026i others(188): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | ATGTATAT others(139): Show |
1 | a0001c0001t0001g0092 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.360+932_360+933ins others(146): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | |||||
chr12:85879483 | A | T | 18 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0035others(15): Show | 25 | HG00738.hp2 HG01361.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.360+914A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879483 | ||||||
chr12:85879493 | T | TATGTATA others(117): Show |
1 | a0001c0001t0001g0094 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.360+1025_360+1026i others(126): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879493 | |||||
chr12:85879514 | T | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(15): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.360+945T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879514 | ||||||
chr12:85879516 | G | GTATATTT others(13): Show |
1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+956_360+975dup others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879516 | |||||
chr12:85879518 | A | ATATTTTA others(115): Show |
1 | a0001c0001t0002g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879518 | |||||
chr12:85879533 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+964A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879533 | ||||||
chr12:85879535 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+966A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879535 | ||||||
chr12:85879536 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+967A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879536 | ||||||
chr12:85879545 | T | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0001g0166others(1): Show | 4 | HG00639.hp2 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+976T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879545 | ||||||
chr12:85879545 | T | TTGTATAT others(159): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0100 | 5 | HG02027.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(168): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879545 | |||||
chr12:85879550 | T | C | 1 | a0001c0001t0001g0053 | 2 | HG00733.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.360+981T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879550 | ||||||
chr12:85879562 | A | ATAAAATA others(118): Show |
1 | a0001c0001t0002g0106 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(127): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879562 | |||||
chr12:85879569 | ATATTTTT others(1): Show |
A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1001_360+1008d others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879569 | ||||||
chr12:85879571 | A | ATTTTTTG others(150): Show |
1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+1017_360+1018i others(159): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879571 | |||||
chr12:85879576 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360+1007T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879576 | ||||||
chr12:85879576 | T | TGTATATT others(3): Show |
1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.360+1007_360+1008i others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879576 | ||||||
chr12:85879576 | TTGTATAT others(4): Show |
T | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.360+1026_360+1036d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879576 | |||||
chr12:85879578 | G | A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1009G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879578 | ||||||
chr12:85879587 | A | ATGTATAT others(13): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(25): Show | 58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(22): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | ATGTATAT others(44): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0054others(3): Show | 7 | HG00642.hp2 HG00735.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(53): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | ATGTATAT others(75): Show |
7 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0076others(4): Show | 10 | HG02148.hp2 NA18955.hp2 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(84): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | ATGTATAT others(106): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0131 | 2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.360+1025_360+1026i others(115): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | ATGTATAT others(137): Show |
1 | a0001c0001t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(146): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | ATGTATAT others(148): Show |
1 | a0001c0001t0001g0037 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.360+1025_360+1026i others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | ATGTATAT others(86): Show |
1 | a0001c0001t0011g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(95): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | |||||
chr12:85879587 | A | T | 3 | a0001c0001t0001g0171a0001c0001t0003g0016a0001c0001t0003g0057 | 5 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1018A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879587 | ||||||
chr12:85879589 | G | GTATATAA others(2): Show |
14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879589 | |||||
chr12:85879589 | G | GTATATAA others(95): Show |
1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(104): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879589 | |||||
chr12:85879598 | A | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(12): Show | 32 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.360+1029A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879598 | ||||||
chr12:85879606 | A | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1037A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879606 | ||||||
chr12:85879607 | A | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1038A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879607 | ||||||
chr12:85879608 | A | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1039A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879608 | ||||||
chr12:85879611 | A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1042A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879611 | ||||||
chr12:85879611 | ATATTTTT others(1): Show |
A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1043_360+1050d others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879611 | ||||||
chr12:85879615 | T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1046T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879615 | ||||||
chr12:85879617 | T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1048T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879617 | ||||||
chr12:85879618 | T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(12): Show | 32 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.360+1049T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879618 | ||||||
chr12:85879618 | TTGTATAT others(4): Show |
T | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.360+1068_360+1078d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879618 | |||||
chr12:85879619 | T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(11): Show | 31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1050T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879619 | ||||||
chr12:85879620 | G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(13): Show | 35 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.360+1051G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879620 | ||||||
chr12:85879629 | A | ATGTATAT others(13): Show |
23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(20): Show | 54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.360+1067_360+1068i others(22): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | |||||
chr12:85879629 | A | ATGTATAT others(75): Show |
1 | a0001c0001t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360+1067_360+1068i others(84): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | |||||
chr12:85879629 | A | ATGTATAT others(128): Show |
1 | a0001c0001t0001g0042 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.360+1067_360+1068i others(137): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | |||||
chr12:85879629 | A | ATGTATAT others(24): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0042others(3): Show | 9 | HG01175.hp2 HG01978.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+1164_360+1194d others(33): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | |||||
chr12:85879629 | A | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0051others(13): Show | 35 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.360+1060A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879629 | ||||||
chr12:85879643 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.360+1074T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879643 | ||||||
chr12:85879651 | A | ATATATTT others(4): Show |
1 | a0001c0001t0002g0060 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+1091_360+1101d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879651 | |||||
chr12:85879656 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.360+1087T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879656 | ||||||
chr12:85879660 | T | TTGTATAT others(4): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0035others(9): Show | 15 | HG00438.hp2 HG00738.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+1099_360+1109d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879660 | |||||
chr12:85879660 | T | TTGTATAT others(35): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(5): Show | 25 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.360+1099_360+1140d others(44): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879660 | |||||
chr12:85879687 | T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0174 | 2 | HG00280.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.360+1118T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879687 | ||||||
chr12:85879687 | T | TTTTTTGT others(24): Show |
1 | a0001c0001t0001g0054 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.360+1148_360+1149i others(33): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879687 | |||||
chr12:85879691 | T | TTGTATAT others(4): Show |
30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(27): Show | 53 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.360+1130_360+1140d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879691 | |||||
chr12:85879718 | T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 29 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.360+1149T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879718 | ||||||
chr12:85879718 | T | TTTTTTGT others(24): Show |
13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(10): Show | 29 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.360+1179_360+1180i others(33): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879718 | |||||
chr12:85879718 | T | TTTTTTGT others(97): Show |
1 | a0001c0001t0001g0050 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+1171_360+1172i others(106): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879718 | |||||
chr12:85879733 | A | ATGTATAT others(23): Show |
3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG02109.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.360+1215_360+1244d others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879733 | |||||
chr12:85879749 | T | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0055others(14): Show | 24 | HG00639.hp1 HG01261.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.360+1180T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879749 | ||||||
chr12:85879756 | T | TATATTTT others(25): Show |
1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.360+1194_360+1195i others(34): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879756 | |||||
chr12:85879759 | A | C | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1190A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879759 | ||||||
chr12:85879763 | T | TA | 4 | a0001c0001t0001g0022a0001c0001t0001g0099a0001c0001t0001g0141others(1): Show | 6 | HG02486.hp2 HG03139.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1194_360+1195i others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879763 | ||||||
chr12:85879763 | T | TATGTATA others(25): Show |
1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+1194_360+1195i others(34): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879763 | ||||||
chr12:85879767 | A | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1198A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879767 | ||||||
chr12:85879780 | TTTTTGTA others(2): Show |
T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1216_360+1224d others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879780 | |||||
chr12:85879789 | A | C | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+1220A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879789 | ||||||
chr12:85879793 | T | A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1224T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879793 | ||||||
chr12:85879797 | A | T | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+1228A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879797 | ||||||
chr12:85879799 | ATAAAATA others(3): Show |
A | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1232_360+1241d others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879799 | |||||
chr12:85879813 | TA | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0099a0001c0001t0001g0141others(1): Show | 6 | HG02486.hp2 HG03139.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1245delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879813 | ||||||
chr12:85879824 | TA | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0099a0001c0001t0001g0141others(1): Show | 6 | HG02486.hp2 HG03139.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1256delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879824 | ||||||
chr12:85879841 | T | TTTTTATG others(4): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0099 | 4 | NA18990.hp1 NA19000.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1276_360+1286d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879841 | |||||
chr12:85879841 | T | TTTTTTGT others(34): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.360+1276_360+1277i others(43): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879841 | |||||
chr12:85879907 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.360+1338A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879907 | ||||||
chr12:85880000 | C | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1431C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880000 | ||||||
chr12:85880045 | C | T | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1476C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880045 | ||||||
chr12:85880117 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.360+1548T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880117 | ||||||
chr12:85880364 | T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1795T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880364 | ||||||
chr12:85880365 | C | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 8 | HG02109.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+1796C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880365 | ||||||
chr12:85880379 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.360+1810T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880379 | ||||||
chr12:85880517 | TAAG | T | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-1699_361-1697d others(5): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85880517 | |||||
chr12:85880552 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1671T>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880552 | ||||||
chr12:85880719 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.361-1504G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880719 | ||||||
chr12:85880759 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.361-1464C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880759 | ||||||
chr12:85880760 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.361-1463G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880760 | ||||||
chr12:85880772 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1451G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880772 | ||||||
chr12:85880773 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1450A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880773 | ||||||
chr12:85880776 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1447C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880776 | ||||||
chr12:85880808 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361-1415C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880808 | ||||||
chr12:85880809 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.361-1414G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880809 | ||||||
chr12:85880989 | GA | G | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-1229delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85880989 | |||||
chr12:85881302 | A | G | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-921A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881302 | ||||||
chr12:85881318 | C | T | 2 | a0001c0001t0004g0049a0001c0001t0004g0146 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.361-905C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881318 | ||||||
chr12:85881503 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.361-720T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881503 | ||||||
chr12:85881569 | T | C | 2 | a0001c0001t0003g0016a0001c0001t0003g0057 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-654T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881569 | ||||||
chr12:85881643 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.361-580C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881643 | ||||||
chr12:85881679 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.361-544G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881679 | ||||||
chr12:85881878 | A | G | 3 | a0001c0001t0003g0016a0001c0001t0003g0056a0001c0001t0003g0057 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-345A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881878 | ||||||
chr12:85881965 | A | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.361-258A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881965 | ||||||
chr12:85882041 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-182T>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85882041 |