geneid | 4863 |
---|---|
ensemblid | ENSG00000149308.17 |
hgncid | 7896 |
symbol | NPAT |
name | nuclear protein, coactivator of histone transcription |
refseq_nuc | NM_002519.3 |
refseq_prot | NP_002510.2 |
ensembl_nuc | ENST00000278612.9 |
ensembl_prot | ENSP00000278612.8 |
mane_status | MANE Select |
chr | chr11 |
start | 108157215 |
end | 108222638 |
strand | - |
ver | v1.2 |
region | chr11:108157215-108222638 |
region5000 | chr11:108152215-108227638 |
regionname0 | NPAT_chr11_108157215_108222638 |
regionname5000 | NPAT_chr11_108152215_108227638 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1427 | 188 | 48 | 30 | 79 | 8 | 23 | 64 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002 | 1/0 | 1427 | 88 | 25 | 14 | 39 | 0 | 9 | 29 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0003 | 0/0 | 1427 | 33 | 0 | 5 | 27 | 0 | 1 | 21 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0004 | 0/0 | 1427 | 15 | 13 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0005 | 0/0 | 1427 | 7 | 1 | 0 | 1 | 2 | 3 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0006 | 0/1 | 1427 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0007 | 0/0 | 1427 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0008 | 0/0 | 1427 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0009 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0010 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0011 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0012 | 0/0 | 1427 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0013 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0014 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0015 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0016 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0017 | 0/0 | 1427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0018 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0019 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4284 | 182 | 44 | 30 | 77 | 8 | 23 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0002 | 1/0 | 4284 | 86 | 23 | 14 | 39 | 0 | 9 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0003 | 0/0 | 4284 | 33 | 0 | 5 | 27 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0004 | 0/0 | 4284 | 15 | 13 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0005 | 0/0 | 4284 | 7 | 1 | 0 | 1 | 2 | 3 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0006 | 0/0 | 4284 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0007 | 0/1 | 4284 | 3 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0008 | 0/0 | 4284 | 3 | 0 | 2 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0009 | 0/0 | 4284 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0010 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0011 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0012 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0013 | 0/0 | 4284 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0014 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0015 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0016 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0017 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0018 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0019 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0020 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0021 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0022 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0023 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
c0024 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1831 | 163 | 29 | 27 | 70 | 11 | 25 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0002 | 1/0 | 1830 | 155 | 51 | 24 | 66 | 2 | 11 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0003 | 0/0 | 1831 | 16 | 0 | 5 | 10 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0004 | 0/0 | 1830 | 5 | 5 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0005 | 0/0 | 1831 | 4 | 3 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0006 | 0/0 | 1830 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0007 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0008 | 0/0 | 1831 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0009 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0010 | 0/0 | 1830 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
t0011 | 0/0 | 1831 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4284 | 182 | 44 | 30 | 77 | 8 | 23 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0006 | 0/0 | 4284 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0011 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0016 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0002 | 1/0 | 4284 | 86 | 23 | 14 | 39 | 0 | 9 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0020 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0022 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0003c0003 | 0/0 | 4284 | 33 | 0 | 5 | 27 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0004c0004 | 0/0 | 4284 | 15 | 13 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0005c0005 | 0/0 | 4284 | 7 | 1 | 0 | 1 | 2 | 3 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0006c0007 | 0/1 | 4284 | 3 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0007c0008 | 0/0 | 4284 | 3 | 0 | 2 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0008c0009 | 0/0 | 4284 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0009c0024 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0010c0010 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0011c0023 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0012c0013 | 0/0 | 4284 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0013c0015 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0014c0017 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0015c0018 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0016c0019 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0017c0021 | 0/0 | 4284 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0018c0014 | 0/0 | 4284 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0019c0012 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6114 | 142 | 24 | 23 | 66 | 8 | 21 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0001t0002 | 0/0 | 6113 | 18 | 16 | 1 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0001t0003 | 0/0 | 6114 | 15 | 0 | 5 | 10 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0001t0005 | 0/0 | 6114 | 4 | 3 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0001t0008 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0001t0009 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0001t0011 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0006t0001 | 0/0 | 6114 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0011t0001 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0001c0016t0001 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0002t0002 | 1/0 | 6113 | 78 | 18 | 13 | 37 | 0 | 9 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0002t0004 | 0/0 | 6113 | 4 | 4 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0002t0006 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0002t0007 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0002t0010 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0020t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0002c0022t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0003c0003t0002 | 0/0 | 6113 | 33 | 0 | 5 | 27 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0004c0004t0002 | 0/0 | 6113 | 15 | 13 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0005c0005t0001 | 0/0 | 6114 | 7 | 1 | 0 | 1 | 2 | 3 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0006c0007t0001 | 0/1 | 6114 | 3 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0007c0008t0001 | 0/0 | 6114 | 3 | 0 | 2 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0008c0009t0002 | 0/0 | 6113 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0009c0024t0002 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0010c0010t0001 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0011c0023t0003 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0012c0013t0002 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0013c0015t0001 | 0/0 | 6114 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0014c0017t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0015c0018t0002 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0016c0019t0002 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0017c0021t0002 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0018c0014t0002 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
a0019c0012t0004 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | copy fasta | chr11 | 108152215 | 108227638 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0011t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0001c0016t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0002t0010g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0020t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0002c0022t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0003c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0004c0004t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0005c0005t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0005c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0005c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0005c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0005c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0005c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0006c0007t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0006c0007t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0006c0007t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0007c0008t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0007c0008t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0007c0008t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0008c0009t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0008c0009t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0009c0024t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0010c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0011c0023t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0012c0013t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0013c0015t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0014c0017t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0015c0018t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0016c0019t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0017c0021t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0018c0014t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
a0019c0012t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0001 | g0011 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00140 | hp1 | a0005 | c0005 | t0001 | g0072 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00140 | hp2 | a0015 | c0018 | t0002 | g0198 | EUR | GBR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00280 | hp2 | a0011 | c0023 | t0003 | g0092 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00323 | hp2 | a0017 | c0021 | t0002 | g0234 | EUR | FIN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00423 | hp1 | a0003 | c0003 | t0002 | g0283 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00544 | hp1 | a0003 | c0003 | t0002 | g0252 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00544 | hp2 | a0005 | c0005 | t0001 | g0078 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00673 | hp1 | a0003 | c0003 | t0002 | g0223 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | CHS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0246 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00735 | hp1 | a0006 | c0007 | t0001 | g0124 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00735 | hp2 | a0003 | c0003 | t0002 | g0262 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00738 | hp1 | a0007 | c0008 | t0001 | g0101 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00741 | hp1 | a0003 | c0003 | t0002 | g0207 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01070 | hp1 | a0006 | c0007 | t0001 | g0104 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01070 | hp2 | a0004 | c0004 | t0002 | g0307 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01168 | hp2 | a0003 | c0003 | t0002 | g0022 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0022 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01175 | hp2 | a0012 | c0013 | t0002 | g0160 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01243 | hp1 | a0004 | c0004 | t0002 | g0025 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01257 | hp1 | a0007 | c0008 | t0001 | g0099 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0260 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0193 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01515 | hp1 | a0007 | c0008 | t0001 | g0064 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01975 | hp2 | a0008 | c0009 | t0002 | g0293 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02004 | hp2 | a0008 | c0009 | t0002 | g0294 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02040 | hp2 | a0002 | c0002 | t0006 | g0242 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02071 | hp1 | a0002 | c0002 | t0006 | g0279 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02129 | hp1 | a0003 | c0003 | t0002 | g0201 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02132 | hp1 | a0003 | c0003 | t0002 | g0251 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02135 | hp1 | a0003 | c0003 | t0002 | g0281 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02145 | hp2 | a0004 | c0004 | t0002 | g0304 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0258 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02257 | hp2 | a0016 | c0019 | t0002 | g0161 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02258 | hp1 | a0004 | c0004 | t0002 | g0189 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0291 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02451 | hp1 | a0002 | c0022 | t0002 | g0315 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | KHV | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0178 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0216 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0317 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0290 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0292 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02647 | hp2 | a0004 | c0004 | t0002 | g0299 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0295 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02717 | hp1 | a0002 | c0002 | t0004 | g0316 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02717 | hp2 | a0002 | c0002 | t0004 | g0215 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02723 | hp1 | a0004 | c0004 | t0002 | g0303 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02735 | hp1 | a0009 | c0024 | t0002 | g0225 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0278 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0217 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0053 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02897 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | GWD | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02922 | hp2 | a0014 | c0017 | t0002 | g0162 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02970 | hp1 | a0004 | c0004 | t0002 | g0305 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02970 | hp2 | a0019 | c0012 | t0004 | g0218 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02976 | hp2 | a0004 | c0004 | t0002 | g0310 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03098 | hp1 | a0004 | c0004 | t0002 | g0306 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0273 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03225 | hp1 | a0004 | c0004 | t0002 | g0025 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0256 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0209 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03516 | hp2 | a0004 | c0004 | t0002 | g0309 | AFR | ESN | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03579 | hp1 | a0001 | c0006 | t0001 | g0050 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03654 | hp1 | a0005 | c0005 | t0001 | g0115 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03669 | hp2 | a0001 | c0001 | t0008 | g0063 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0268 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03704 | hp2 | a0005 | c0005 | t0001 | g0076 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0232 | SAS | PJL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0231 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03834 | hp2 | a0013 | c0015 | t0001 | g0074 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03927 | hp1 | a0003 | c0003 | t0002 | g0275 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03942 | hp2 | a0001 | c0001 | t0011 | g0165 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0237 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18522 | hp1 | a0004 | c0004 | t0002 | g0302 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18906 | hp2 | a0002 | c0002 | t0007 | g0026 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18939 | hp1 | a0003 | c0003 | t0002 | g0247 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18941 | hp2 | a0003 | c0003 | t0002 | g0210 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18946 | hp1 | a0003 | c0003 | t0002 | g0214 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18948 | hp1 | a0003 | c0003 | t0002 | g0213 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18954 | hp1 | a0001 | c0011 | t0001 | g0036 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18954 | hp2 | a0018 | c0014 | t0002 | g0197 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18961 | hp1 | a0003 | c0003 | t0002 | g0284 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18964 | hp2 | a0001 | c0016 | t0001 | g0133 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18970 | hp1 | a0003 | c0003 | t0002 | g0280 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18977 | hp1 | a0003 | c0003 | t0002 | g0250 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18982 | hp1 | a0003 | c0003 | t0002 | g0249 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18983 | hp1 | a0003 | c0003 | t0002 | g0288 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18984 | hp2 | a0003 | c0003 | t0002 | g0222 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18985 | hp1 | a0003 | c0003 | t0002 | g0286 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18986 | hp1 | a0003 | c0003 | t0002 | g0211 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18992 | hp2 | a0003 | c0003 | t0002 | g0212 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19003 | hp2 | a0003 | c0003 | t0002 | g0208 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19004 | hp1 | a0010 | c0010 | t0001 | g0129 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19005 | hp2 | a0003 | c0003 | t0002 | g0248 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19058 | hp1 | a0003 | c0003 | t0002 | g0255 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19067 | hp1 | a0003 | c0003 | t0002 | g0271 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19068 | hp2 | a0003 | c0003 | t0002 | g0287 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19078 | hp2 | a0003 | c0003 | t0002 | g0254 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19085 | hp2 | a0003 | c0003 | t0002 | g0253 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0245 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA19240 | hp2 | a0001 | c0006 | t0001 | g0051 | AFR | YRI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20129 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | ASW | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ASW | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20905 | hp1 | a0005 | c0005 | t0001 | g0055 | SAS | GIH | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG01123 | hp2 | a0002 | c0002 | t0010 | g0282 | AMR | CLM | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02109 | hp1 | a0004 | c0004 | t0002 | g0308 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02559 | hp1 | a0004 | c0004 | t0002 | g0301 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG03471 | hp2 | a0002 | c0020 | t0002 | g0202 | AFR | MSL | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18955 | hp1 | a0003 | c0003 | t0002 | g0285 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0265 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
NA21309 | hp2 | a0004 | c0004 | t0002 | g0300 | AFR | LWK | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
homoSapiens_chm13v2 | hp1 | a0006 | c0007 | t0001 | g0100 | REF | REF | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0269 | REF | REF | NPAT_chr11_108152215_108227638 | NPAT | chr11 | 108152215 | 108227638 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:108161506
|
C | A | 1 | a0017 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.3580G>T | p.Gly1194Cys | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3682/6113 | 3580/4284 | 1194/1427 | chr11 | 108161506 | ||
chr11:108161887
|
C | T | 1 | a0015 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.3199G>A | p.Asp1067Asn | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3301/6113 | 3199/4284 | 1067/1427 | chr11 | 108161887 | ||
chr11:108161949
|
G | A | 1 | a0007 | 3 | HG00738.hp1 HG01257.hp1 HG01515.hp1 |
missense_variant | MODERATE | c.3137C>T | p.Pro1046Leu | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3239/6113 | 3137/4284 | 1046/1427 | chr11 | 108161949 | ||
chr11:108161980
|
G | T | 1 | a0006 | 3 | HG00735.hp1 HG01070.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.3106C>A | p.Leu1036Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 3208/6113 | 3106/4284 | 1036/1427 | chr11 | 108161980 | ||
chr11:108169757
|
G | T | 2 | a0005a0013 | 8 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(5): Show |
missense_variant | MODERATE | c.2997C>A | p.Asn999Lys | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/18 | 3099/6113 | 2997/4284 | 999/1427 | chr11 | 108169757 | ||
chr11:108169795
|
C | T | 1 | a0012 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2959G>A | p.Val987Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/18 | 3061/6113 | 2959/4284 | 987/1427 | chr11 | 108169795 | ||
chr11:108169835
|
C | G | 1 | a0014 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.2919G>C | p.Leu973Phe | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/18 | 3021/6113 | 2919/4284 | 973/1427 | chr11 | 108169835 | ||
chr11:108172566
|
A | C | 1 | a0016 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2418T>G | p.Asp806Glu | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 2520/6113 | 2418/4284 | 806/1427 | chr11 | 108172566 | ||
chr11:108173122
|
A | G | 1 | a0013 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1862T>C | p.Val621Ala | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1964/6113 | 1862/4284 | 621/1427 | chr11 | 108173122 | ||
chr11:108173161
|
A | G | 1 | a0004 | 15 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
missense_variant | MODERATE | c.1823T>C | p.Val608Ala | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1925/6113 | 1823/4284 | 608/1427 | chr11 | 108173161 | ||
chr11:108173261
|
C | T | 13 | a0001a0004a0005others(10): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
missense_variant | MODERATE | c.1723G>A | p.Val575Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1825/6113 | 1723/4284 | 575/1427 | chr11 | 108173261 | ||
chr11:108173364
|
T | A | 2 | a0003a0009 | 34 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(31): Show |
missense_variant | MODERATE | c.1620A>T | p.Leu540Phe | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1722/6113 | 1620/4284 | 540/1427 | chr11 | 108173364 | ||
chr11:108173636
|
A | C | 1 | a0018 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1348T>G | p.Leu450Val | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1450/6113 | 1348/4284 | 450/1427 | chr11 | 108173636 | ||
chr11:108173645
|
C | T | 1 | a0012 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1339G>A | p.Val447Met | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1441/6113 | 1339/4284 | 447/1427 | chr11 | 108173645 | ||
chr11:108186499
|
C | T | 1 | a0019 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.709G>A | p.Ala237Thr | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/18 | 811/6113 | 709/4284 | 237/1427 | chr11 | 108186499 | ||
chr11:108189274
|
T | C | 1 | a0011 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.388A>G | p.Thr130Ala | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/18 | 490/6113 | 388/4284 | 130/1427 | chr11 | 108189274 | ||
chr11:108190498
|
C | T | 1 | a0010 | 1 | NA19004.hp1 | missense_variant&splice_region_variant | MODERATE | c.293G>A | p.Ser98Asn | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/18 | 395/6113 | 293/4284 | 98/1427 | chr11 | 108190498 | ||
chr11:108192127
|
G | C | 1 | a0009 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.281C>G | p.Ser94Cys | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/18 | 383/6113 | 281/4284 | 94/1427 | chr11 | 108192127 | ||
chr11:108194004
|
T | C | 1 | a0008 | 2 | HG01975.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.170A>G | p.Lys57Arg | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/18 | 272/6113 | 170/4284 | 57/1427 | chr11 | 108194004 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:108161153
|
T | C | 1 | a0001c0006 | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.3933A>G | p.Pro1311Pro | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/18 | 4035/6113 | 3933/4284 | 1311/1427 | chr11 | 108161153 | ||
chr11:108172920
|
C | T | 1 | a0002c0020 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2064G>A | p.Thr688Thr | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 2166/6113 | 2064/4284 | 688/1427 | chr11 | 108172920 | ||
chr11:108173100
|
C | T | 1 | a0001c0016 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1884G>A | p.Ser628Ser | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1986/6113 | 1884/4284 | 628/1427 | chr11 | 108173100 | ||
chr11:108173127
|
T | C | 1 | a0016c0019 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1857A>G | p.Gly619Gly | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/18 | 1959/6113 | 1857/4284 | 619/1427 | chr11 | 108173127 | ||
chr11:108185307
|
A | G | 1 | a0001c0006 | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.831T>C | p.Ile277Ile | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/18 | 933/6113 | 831/4284 | 277/1427 | chr11 | 108185307 | ||
chr11:108185471
|
T | C | 1 | a0002c0022 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.750A>G | p.Arg250Arg | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 9/18 | 852/6113 | 750/4284 | 250/1427 | chr11 | 108185471 | ||
chr11:108189158
|
C | T | 1 | a0001c0011 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.504G>A | p.Ser168Ser | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/18 | 606/6113 | 504/4284 | 168/1427 | chr11 | 108189158 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:108157292
|
T | C | 1 | a0001c0001t0009 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1650A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 1650 | chr11 | 108157292 | |||||
chr11:108157329
|
T | C | 1 | a0001c0001t0005 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1613A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 1613 | chr11 | 108157329 | |||||
chr11:108157433
|
C | T | 1 | a0002c0002t0006 | 2 | HG02040.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1509G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 1509 | chr11 | 108157433 | |||||
chr11:108157943
|
T | C | 2 | a0001c0001t0003a0011c0023t0003 | 16 | HG00280.hp2 HG01496.hp1 HG01952.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*999A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 999 | chr11 | 108157943 | |||||
chr11:108158206
|
T | C | 2 | a0002c0002t0004a0019c0012t0004 | 5 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*736A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 736 | chr11 | 108158206 | |||||
chr11:108158257
|
T | G | 1 | a0002c0002t0010 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*685A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 685 | chr11 | 108158257 | |||||
chr11:108158382
|
T | TA | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(11): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*559dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 559 | chr11 | 108158382 | |||||
chr11:108158431
|
A | G | 1 | a0001c0001t0008 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 511 | chr11 | 108158431 | |||||
chr11:108158813
|
T | C | 1 | a0001c0001t0011 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 18/18 | 129 | chr11 | 108158813 | |||||
chr11:108222611
|
C | T | 1 | a0002c0002t0007 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/18 | 75 | chr11 | 108222611 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:108159474
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4207-455T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159474 | ||||||
chr11:108159630
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0065others(6): Show | 10 | HG01934.hp2 HG02004.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.4207-611G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159630 | ||||||
chr11:108159858
|
A | C | 1 | a0012c0013t0002g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4207-839T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159858 | ||||||
chr11:108159860
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.4207-841G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159860 | ||||||
chr11:108159877
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4207-858C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159877 | ||||||
chr11:108159886
|
C | T | 3 | a0004c0004t0002g0307a0004c0004t0002g0308a0004c0004t0002g0309 | 3 | HG01070.hp2 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4207-867G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159886 | ||||||
chr11:108159968
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4206+912G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108159968 | ||||||
chr11:108160015
|
G | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.4206+865C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160015 | ||||||
chr11:108160106
|
C | T | 1 | a0002c0002t0002g0241 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4206+774G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160106 | ||||||
chr11:108160147
|
C | CA | 21 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0075others(18): Show | 23 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.4206+732dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160147 | ||||||
chr11:108160395
|
T | C | 1 | a0001c0011t0001g0036 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4206+485A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160395 | ||||||
chr11:108160435
|
C | G | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(312): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.4206+445G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160435 | ||||||
chr11:108160567
|
TC | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(137): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.4206+312delG | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160567 | ||||||
chr11:108160568
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 63 | HG01070.hp2 HG01109.hp2 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.4206+312G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160568 | ||||||
chr11:108160572
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4206+308A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160572 | ||||||
chr11:108160649
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(13): Show | 19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.4206+231C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160649 | ||||||
chr11:108160684
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4206+196G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 17/17 | chr11 | 108160684 | ||||||
chr11:108162312
|
T | C | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-132A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162312 | ||||||
chr11:108162392
|
T | C | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-212A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162392 | ||||||
chr11:108162465
|
C | CT | 5 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3011-286dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162465 | ||||||
chr11:108162494
|
G | A | 1 | a0002c0002t0002g0259 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3011-314C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162494 | ||||||
chr11:108162555
|
C | T | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-375G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162555 | ||||||
chr11:108162685
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3011-505C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162685 | ||||||
chr11:108162766
|
A | G | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3011-586T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162766 | ||||||
chr11:108162842
|
T | C | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3011-662A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108162842 | ||||||
chr11:108163059
|
G | GATTT | 34 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0042others(31): Show | 36 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.3011-883_3011-880d others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | ||||||
chr11:108163059
|
G | GATTTATT others(1): Show |
29 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(26): Show | 33 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.3011-887_3011-880d others(10): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | ||||||
chr11:108163059
|
G | GATTTATT others(5): Show |
14 | a0001c0001t0001g0153a0001c0001t0002g0180a0001c0001t0002g0181others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.3011-891_3011-880d others(14): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | ||||||
chr11:108163059
|
G | GATTTATT others(9): Show |
1 | a0001c0001t0002g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3011-895_3011-880d others(18): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | ||||||
chr11:108163059
|
GATTT | G | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-883_3011-880d others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163059 | ||||||
chr11:108163067
|
T | C | 1 | a0003c0003t0002g0285 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3011-887A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163067 | ||||||
chr11:108163103
|
G | A | 42 | a0002c0002t0002g0002a0002c0002t0002g0021a0002c0002t0002g0191others(39): Show | 46 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.3011-923C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163103 | ||||||
chr11:108163169
|
TC | T | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-990delG | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163169 | ||||||
chr11:108163228
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(138): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.3011-1048G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163228 | ||||||
chr11:108163229
|
G | A | 4 | a0002c0002t0002g0229a0002c0002t0002g0235a0002c0002t0002g0276others(1): Show | 4 | NA18953.hp1 NA18960.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-1049C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163229 | ||||||
chr11:108163285
|
A | G | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.3011-1105T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163285 | ||||||
chr11:108163315
|
A | G | 2 | a0002c0002t0002g0230a0002c0002t0002g0263 | 2 | NA18973.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3011-1135T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163315 | ||||||
chr11:108163397
|
A | G | 100 | a0002c0002t0002g0002a0002c0002t0002g0019a0002c0002t0002g0020others(97): Show | 108 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3011-1217T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163397 | ||||||
chr11:108163446
|
A | G | 1 | a0001c0006t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3011-1266T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163446 | ||||||
chr11:108163572
|
A | G | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-1392T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163572 | ||||||
chr11:108163822
|
G | GA | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.3011-1643_3011-164 others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108163822 | ||||||
chr11:108164049
|
T | C | 1 | a0002c0002t0007g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3011-1869A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164049 | ||||||
chr11:108164380
|
T | C | 1 | a0002c0002t0002g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3011-2200A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164380 | ||||||
chr11:108164404
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3011-2224C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164404 | ||||||
chr11:108164484
|
C | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0029others(6): Show | 11 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3011-2304G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164484 | ||||||
chr11:108164617
|
A | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.3011-2437T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164617 | ||||||
chr11:108164882
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3011-2702C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164882 | ||||||
chr11:108164925
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3011-2745A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164925 | ||||||
chr11:108164987
|
C | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3011-2807G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108164987 | ||||||
chr11:108165346
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0081others(14): Show | 18 | HG00438.hp2 HG02135.hp2 NA18941.hp1 others(15): Show |
intron_variant | MODIFIER | c.3011-3166C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165346 | ||||||
chr11:108165375
|
G | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3011-3195C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165375 | ||||||
chr11:108165452
|
T | TTA | 53 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.3011-3274_3011-327 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165452 | ||||||
chr11:108165452
|
T | TTATA | 10 | a0001c0001t0001g0057a0001c0001t0001g0077a0001c0001t0001g0083others(7): Show | 10 | HG00733.hp1 HG01261.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.3011-3276_3011-327 others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165452 | ||||||
chr11:108165454
|
A | T | 1 | a0012c0013t0002g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3011-3274T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165454 | ||||||
chr11:108165466
|
A | AT | 4 | a0001c0001t0001g0144a0001c0001t0001g0172a0001c0006t0001g0053others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-3287dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165466 | ||||||
chr11:108165468
|
A | AT | 20 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0035others(17): Show | 23 | HG01978.hp2 HG02132.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.3011-3289dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165468 | ||||||
chr11:108165468
|
A | T | 9 | a0001c0001t0001g0144a0001c0001t0001g0164a0001c0001t0001g0172others(6): Show | 10 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3011-3288T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165468 | ||||||
chr11:108165470
|
A | AT | 23 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.3011-3291dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | ||||||
chr11:108165470
|
A | ATT | 4 | a0001c0001t0002g0179a0001c0001t0002g0200a0001c0001t0005g0040others(1): Show | 4 | HG01255.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-3291_3011-329 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | ||||||
chr11:108165470
|
A | ATTT | 3 | a0001c0001t0001g0049a0001c0001t0002g0184a0001c0001t0002g0311 | 3 | HG02622.hp2 HG03486.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3011-3291_3011-329 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | ||||||
chr11:108165470
|
A | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0035others(37): Show | 44 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.3011-3290T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165470 | ||||||
chr11:108165472
|
A | AT | 32 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(29): Show | 34 | HG00438.hp1 HG00558.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.3011-3293dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165472
|
A | ATAT | 11 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0150others(8): Show | 13 | HG00558.hp2 HG00639.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3011-3293_3011-329 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165472
|
A | ATATT | 6 | a0001c0001t0002g0183a0001c0001t0002g0190a0001c0001t0002g0296others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3011-3293_3011-329 others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165472
|
A | ATT | 28 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(25): Show | 31 | HG00140.hp2 HG00438.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.3011-3294_3011-329 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165472
|
A | ATTT | 7 | a0001c0001t0001g0017a0001c0001t0001g0148a0001c0001t0001g0149others(4): Show | 8 | HG01081.hp2 HG02055.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.3011-3295_3011-329 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165472
|
A | ATTTT | 11 | a0004c0004t0002g0025a0004c0004t0002g0300a0004c0004t0002g0301others(8): Show | 12 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3011-3296_3011-329 others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165472
|
A | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.3011-3292T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165472 | ||||||
chr11:108165473
|
T | TA | 4 | a0001c0001t0001g0118a0006c0007t0001g0100a0006c0007t0001g0104others(1): Show | 4 | HG00735.hp1 HG01070.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-3294_3011-329 others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165473 | ||||||
chr11:108165475
|
T | A | 1 | a0006c0007t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3011-3295A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165475 | ||||||
chr11:108165635
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3011-3455A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165635 | ||||||
chr11:108165663
|
C | T | 1 | a0002c0002t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3011-3483G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165663 | ||||||
chr11:108165756
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-3576G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165756 | ||||||
chr11:108165773
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3011-3593T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165773 | ||||||
chr11:108165951
|
T | A | 32 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(29): Show | 34 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.3011-3771A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108165951 | ||||||
chr11:108166017
|
C | CA | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(314): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.3010+3726dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166017 | ||||||
chr11:108166023
|
T | G | 4 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3010+3721A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166023 | ||||||
chr11:108166065
|
G | A | 3 | a0001c0001t0002g0199a0015c0018t0002g0198a0018c0014t0002g0197 | 3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3010+3679C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166065 | ||||||
chr11:108166302
|
G | T | 1 | a0002c0002t0002g0298 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3010+3442C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166302 | ||||||
chr11:108166353
|
C | T | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010+3391G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166353 | ||||||
chr11:108166401
|
T | A | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010+3343A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166401 | ||||||
chr11:108166405
|
A | T | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010+3339T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166405 | ||||||
chr11:108166631
|
T | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.3010+3113A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108166631 | ||||||
chr11:108167081
|
A | G | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3010+2663T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167081 | ||||||
chr11:108167353
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3010+2391A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167353 | ||||||
chr11:108167415
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.3010+2329T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167415 | ||||||
chr11:108167599
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3010+2145C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167599 | ||||||
chr11:108167750
|
A | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(97): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.3010+1994T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167750 | ||||||
chr11:108167816
|
T | C | 10 | a0001c0001t0002g0199a0001c0001t0002g0200a0002c0002t0004g0215others(7): Show | 10 | HG00140.hp2 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3010+1928A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167816 | ||||||
chr11:108167923
|
C | T | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3010+1821G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108167923 | ||||||
chr11:108168134
|
G | A | 1 | a0009c0024t0002g0225 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3010+1610C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168134 | ||||||
chr11:108168159
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3010+1585A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168159 | ||||||
chr11:108168160
|
ACTT | A | 11 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3010+1581_3010+158 others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168160 | ||||||
chr11:108168209
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3010+1535G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168209 | ||||||
chr11:108168211
|
C | T | 3 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3010+1533G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168211 | ||||||
chr11:108168315
|
T | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0149others(8): Show | 13 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.3010+1429A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168315 | ||||||
chr11:108168321
|
A | G | 27 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(24): Show | 28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3010+1423T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168321 | ||||||
chr11:108168414
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3010+1330T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168414 | ||||||
chr11:108168557
|
T | C | 2 | a0002c0002t0002g0240a0002c0002t0002g0278 | 2 | HG01257.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3010+1187A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168557 | ||||||
chr11:108168705
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(11): Show | 15 | HG02132.hp2 HG02451.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.3010+1039G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168705 | ||||||
chr11:108168773
|
A | G | 8 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3010+971T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168773 | ||||||
chr11:108168835
|
T | C | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010+909A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168835 | ||||||
chr11:108168868
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3010+876A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168868 | ||||||
chr11:108168889
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3010+855G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108168889 | ||||||
chr11:108169254
|
C | T | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3010+490G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169254 | ||||||
chr11:108169377
|
A | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.3010+367T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169377 | ||||||
chr11:108169546
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3010+198G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169546 | ||||||
chr11:108169554
|
G | A | 1 | a0012c0013t0002g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3010+190C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169554 | ||||||
chr11:108169688
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0120 | 3 | HG02523.hp1 NA18973.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3010+56C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 15/17 | chr11 | 108169688 | ||||||
chr11:108170521
|
AG | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.2786-479delC | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108170521 | ||||||
chr11:108170523
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2786-480C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108170523 | ||||||
chr11:108171089
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 17 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.2786-1046C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171089 | ||||||
chr11:108171114
|
T | C | 1 | a0002c0002t0002g0020 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2786-1071A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171114 | ||||||
chr11:108171124
|
A | AT | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2785+1074dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | ||||||
chr11:108171124
|
A | ATT | 35 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(32): Show | 35 | HG00408.hp2 HG00642.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.2785+1073_2785+107 others(6): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | ||||||
chr11:108171124
|
AT | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 17 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.2785+1074delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | ||||||
chr11:108171124
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0134 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2785+1064_2785+107 others(15): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171124 | ||||||
chr11:108171170
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2785+1029T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171170 | ||||||
chr11:108171193
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2785+1006G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171193 | ||||||
chr11:108171240
|
G | C | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2785+959C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171240 | ||||||
chr11:108171312
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2785+887C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171312 | ||||||
chr11:108171368
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2785+831G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171368 | ||||||
chr11:108171473
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2785+726C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171473 | ||||||
chr11:108171486
|
G | GT | 12 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0134others(9): Show | 14 | HG02602.hp2 HG03688.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.2785+712dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171486 | ||||||
chr11:108171486
|
GT | G | 7 | a0001c0001t0001g0082a0001c0001t0002g0163a0001c0001t0002g0186others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2785+712delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171486 | ||||||
chr11:108171692
|
C | G | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2785+507G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171692 | ||||||
chr11:108171732
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2785+467G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171732 | ||||||
chr11:108171742
|
C | T | 10 | a0001c0001t0001g0158a0003c0003t0002g0208a0003c0003t0002g0222others(7): Show | 10 | HG00544.hp1 HG02735.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.2785+457G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171742 | ||||||
chr11:108171814
|
T | C | 1 | a0001c0001t0003g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2785+385A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171814 | ||||||
chr11:108171999
|
C | T | 1 | a0002c0002t0002g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2785+200G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 13/17 | chr11 | 108171999 | ||||||
chr11:108174007
|
T | C | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-156A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174007 | ||||||
chr11:108174268
|
A | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(113): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1133-417T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174268 | ||||||
chr11:108174564
|
T | TA | 22 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0139others(19): Show | 23 | HG00673.hp2 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1133-714dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174564 | ||||||
chr11:108174564
|
TA | T | 11 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0108others(8): Show | 11 | HG00140.hp2 HG01070.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1133-714delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174564 | ||||||
chr11:108174564
|
TAAAAAAA others(3): Show |
T | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1133-723_1133-714d others(12): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174564 | ||||||
chr11:108174586
|
GTATGATA | G | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1133-742_1133-736d others(9): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174586 | ||||||
chr11:108174615
|
C | CT | 7 | a0001c0001t0001g0070a0001c0001t0001g0139a0001c0001t0001g0150others(4): Show | 7 | HG01169.hp2 HG01517.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1133-765dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174615 | ||||||
chr11:108174615
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 8 | NA18939.hp2 NA18953.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.1133-764G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174615 | ||||||
chr11:108174715
|
T | C | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1133-864A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174715 | ||||||
chr11:108174769
|
C | A | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-918G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174769 | ||||||
chr11:108174770
|
C | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-919G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174770 | ||||||
chr11:108174771
|
ACCACAC | A | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-926_1133-921d others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174771 | ||||||
chr11:108174785
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-934C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174785 | ||||||
chr11:108174795
|
T | C | 1 | a0002c0002t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1133-944A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174795 | ||||||
chr11:108174916
|
G | C | 3 | a0001c0001t0002g0163a0014c0017t0002g0162a0016c0019t0002g0161 | 3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1133-1065C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174916 | ||||||
chr11:108174983
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1133-1132C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108174983 | ||||||
chr11:108175226
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1132+1020A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175226 | ||||||
chr11:108175229
|
C | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(142): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1132+1017G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175229 | ||||||
chr11:108175327
|
G | T | 1 | a0001c0001t0003g0114 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1132+919C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175327 | ||||||
chr11:108175425
|
T | C | 3 | a0001c0001t0002g0199a0015c0018t0002g0198a0018c0014t0002g0197 | 3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1132+821A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175425 | ||||||
chr11:108175462
|
T | A | 1 | a0002c0002t0002g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1132+784A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175462 | ||||||
chr11:108175498
|
T | A | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1132+748A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175498 | ||||||
chr11:108175730
|
T | C | 9 | a0003c0003t0002g0208a0003c0003t0002g0222a0003c0003t0002g0247others(6): Show | 9 | HG00544.hp1 NA18939.hp1 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132+516A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 12/17 | chr11 | 108175730 | ||||||
chr11:108176600
|
G | C | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1004-226C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176600 | ||||||
chr11:108176680
|
A | AT | 15 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1004-307dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176680 | ||||||
chr11:108176702
|
G | A | 1 | a0003c0003t0002g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1003+292C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176702 | ||||||
chr11:108176769
|
A | G | 5 | a0001c0001t0002g0181a0001c0006t0001g0050a0001c0006t0001g0051others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003+225T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176769 | ||||||
chr11:108176900
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1003+94T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176900 | ||||||
chr11:108176974
|
GAAAT | G | 4 | a0001c0001t0003g0086a0001c0001t0003g0089a0001c0001t0003g0113others(1): Show | 4 | HG02451.hp1 NA18955.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003+16_1003+19del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 11/17 | chr11 | 108176974 | ||||||
chr11:108177118
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.907-28A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177118 | ||||||
chr11:108177153
|
T | G | 1 | a0006c0007t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.907-63A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177153 | ||||||
chr11:108177187
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.907-97T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177187 | ||||||
chr11:108177210
|
GGTA | G | 5 | a0002c0002t0002g0024a0002c0002t0002g0209a0002c0002t0002g0290others(2): Show | 6 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-123_907-121del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177210 | ||||||
chr11:108177255
|
A | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.907-165T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177255 | ||||||
chr11:108177494
|
G | T | 1 | a0002c0002t0002g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.907-404C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177494 | ||||||
chr11:108177656
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00280.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.907-566T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177656 | ||||||
chr11:108177719
|
CT | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.907-630delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177719 | ||||||
chr11:108177814
|
G | A | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.907-724C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177814 | ||||||
chr11:108177948
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.907-858A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108177948 | ||||||
chr11:108178002
|
T | G | 1 | a0007c0008t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.907-912A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178002 | ||||||
chr11:108178027
|
A | T | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-937T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178027 | ||||||
chr11:108178172
|
T | C | 1 | a0003c0003t0002g0022 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.907-1082A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178172 | ||||||
chr11:108178370
|
G | T | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.907-1280C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178370 | ||||||
chr11:108178377
|
G | A | 9 | a0001c0001t0002g0180a0001c0001t0002g0182a0001c0001t0002g0183others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.907-1287C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178377 | ||||||
chr11:108178409
|
C | T | 3 | a0001c0001t0002g0163a0014c0017t0002g0162a0016c0019t0002g0161 | 3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-1319G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178409 | ||||||
chr11:108178422
|
T | G | 1 | a0001c0001t0002g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907-1332A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178422 | ||||||
chr11:108178422
|
T | TTG | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1334_907-1333d others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178422 | ||||||
chr11:108178566
|
A | G | 3 | a0001c0001t0002g0163a0014c0017t0002g0162a0016c0019t0002g0161 | 3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-1476T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178566 | ||||||
chr11:108178581
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907-1491T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178581 | ||||||
chr11:108178770
|
A | G | 4 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1680T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178770 | ||||||
chr11:108178932
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1842C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108178932 | ||||||
chr11:108179001
|
G | A | 1 | a0005c0005t0001g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.907-1911C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179001 | ||||||
chr11:108179088
|
G | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0169 | 2 | NA18970.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.907-1998C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179088 | ||||||
chr11:108179206
|
C | A | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.907-2116G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179206 | ||||||
chr11:108179328
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.907-2238G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179328 | ||||||
chr11:108179625
|
C | T | 1 | a0002c0002t0002g0298 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.907-2535G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179625 | ||||||
chr11:108179672
|
G | C | 1 | a0005c0005t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.907-2582C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179672 | ||||||
chr11:108179677
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.907-2587C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179677 | ||||||
chr11:108179724
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.907-2634C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179724 | ||||||
chr11:108179766
|
T | C | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.907-2676A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179766 | ||||||
chr11:108179782
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.907-2692G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179782 | ||||||
chr11:108179860
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.907-2770C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108179860 | ||||||
chr11:108180056
|
G | A | 3 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.907-2966C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180056 | ||||||
chr11:108180222
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.907-3132C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180222 | ||||||
chr11:108180385
|
C | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.907-3295G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180385 | ||||||
chr11:108180417
|
A | G | 1 | a0003c0003t0002g0248 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.907-3327T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180417 | ||||||
chr11:108180542
|
C | CAAAAAAT others(299): Show |
1 | a0001c0001t0002g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.907-3453_907-3452i others(308): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180542 | ||||||
chr11:108180542
|
C | CAAAAAAT others(300): Show |
1 | a0001c0001t0002g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.907-3453_907-3452i others(309): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180542 | ||||||
chr11:108180542
|
C | CAAAAAAT others(301): Show |
1 | a0001c0001t0009g0178 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.907-3453_907-3452i others(310): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180542 | ||||||
chr11:108180573
|
A | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.907-3483T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180573 | ||||||
chr11:108180757
|
T | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.907-3667A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180757 | ||||||
chr11:108180978
|
A | G | 14 | a0001c0001t0002g0311a0004c0004t0002g0025a0004c0004t0002g0299others(11): Show | 15 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.907-3888T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108180978 | ||||||
chr11:108181025
|
G | T | 2 | a0003c0003t0002g0286a0003c0003t0002g0287 | 2 | NA18985.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.907-3935C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181025 | ||||||
chr11:108181124
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.907-4034T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181124 | ||||||
chr11:108181235
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.906+3997C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181235 | ||||||
chr11:108181262
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(95): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.906+3970C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181262 | ||||||
chr11:108181275
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.906+3957G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181275 | ||||||
chr11:108181291
|
C | T | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+3941G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181291 | ||||||
chr11:108181325
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.906+3907G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181325 | ||||||
chr11:108181357
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.906+3875A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181357 | ||||||
chr11:108181380
|
G | A | 1 | a0002c0002t0002g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.906+3852C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181380 | ||||||
chr11:108181464
|
C | CA | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.906+3767dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181464 | ||||||
chr11:108181532
|
A | C | 2 | a0001c0001t0002g0190a0004c0004t0002g0189 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.906+3700T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181532 | ||||||
chr11:108181547
|
T | G | 1 | a0002c0002t0002g0289 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.906+3685A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181547 | ||||||
chr11:108181572
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.906+3660A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181572 | ||||||
chr11:108181690
|
A | C | 1 | a0001c0001t0003g0113 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.906+3542T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181690 | ||||||
chr11:108181701
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(13): Show | 19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.906+3531C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181701 | ||||||
chr11:108181737
|
T | TA | 46 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0038others(43): Show | 52 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.906+3494dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181737 | ||||||
chr11:108181984
|
T | C | 1 | a0003c0003t0002g0022 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.906+3248A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108181984 | ||||||
chr11:108182020
|
T | C | 1 | a0004c0004t0002g0307 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.906+3212A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182020 | ||||||
chr11:108182188
|
T | G | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+3044A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182188 | ||||||
chr11:108182202
|
C | G | 1 | a0002c0002t0002g0228 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.906+3030G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182202 | ||||||
chr11:108182261
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906+2971G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182261 | ||||||
chr11:108182419
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0164a0001c0001t0001g0168others(6): Show | 11 | HG02602.hp2 HG03688.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.906+2813A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182419 | ||||||
chr11:108182542
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.906+2690G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182542 | ||||||
chr11:108182566
|
C | T | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+2666G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182566 | ||||||
chr11:108182770
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.906+2462C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182770 | ||||||
chr11:108182930
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.906+2302T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182930 | ||||||
chr11:108182930
|
AAAC | A | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+2299_906+2301d others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108182930 | ||||||
chr11:108183041
|
T | C | 1 | a0002c0002t0002g0298 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.906+2191A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183041 | ||||||
chr11:108183160
|
T | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(139): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.906+2072A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183160 | ||||||
chr11:108183161
|
T | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0089 | 2 | NA18955.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.906+2071A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183161 | ||||||
chr11:108183247
|
A | C | 1 | a0005c0005t0001g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+1985T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183247 | ||||||
chr11:108183355
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(8): Show | 13 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+1877T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183355 | ||||||
chr11:108183581
|
C | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0094a0001c0001t0001g0103 | 3 | NA18950.hp2 NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.906+1651G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183581 | ||||||
chr11:108183673
|
A | C | 11 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+1559T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183673 | ||||||
chr11:108183773
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.906+1459A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183773 | ||||||
chr11:108183781
|
C | A | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.906+1451G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183781 | ||||||
chr11:108183855
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.906+1377G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183855 | ||||||
chr11:108183871
|
G | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906+1361C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183871 | ||||||
chr11:108183877
|
A | G | 208 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.906+1355T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183877 | ||||||
chr11:108183895
|
C | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+1337G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183895 | ||||||
chr11:108183939
|
A | G | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906+1293T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183939 | ||||||
chr11:108183973
|
C | CA | 298 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(295): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.906+1258dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183973 | ||||||
chr11:108183973
|
C | CAA | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.906+1257_906+1258d others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183973 | ||||||
chr11:108183991
|
T | G | 1 | a0002c0002t0010g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.906+1241A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108183991 | ||||||
chr11:108184017
|
C | A | 4 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1215G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184017 | ||||||
chr11:108184070
|
T | A | 1 | a0001c0001t0001g0006 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.906+1162A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184070 | ||||||
chr11:108184080
|
T | C | 1 | a0002c0002t0002g0278 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.906+1152A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184080 | ||||||
chr11:108184195
|
G | A | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.906+1037C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184195 | ||||||
chr11:108184195
|
G | C | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.906+1037C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184195 | ||||||
chr11:108184344
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0029others(5): Show | 10 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.906+888G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184344 | ||||||
chr11:108184405
|
G | C | 3 | a0002c0002t0002g0256a0002c0002t0002g0257a0002c0002t0002g0259 | 3 | HG01496.hp2 HG02523.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.906+827C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184405 | ||||||
chr11:108184407
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906+825C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184407 | ||||||
chr11:108184451
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.906+781C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184451 | ||||||
chr11:108184471
|
C | CA | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(49): Show | 60 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.906+760dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184471 | ||||||
chr11:108184471
|
C | CAA | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(110): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.906+759_906+760dup others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184471 | ||||||
chr11:108184531
|
A | ATCT | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.906+700_906+701ins others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184531 | ||||||
chr11:108184627
|
A | G | 1 | a0002c0002t0002g0295 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.906+605T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184627 | ||||||
chr11:108184677
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.906+555A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184677 | ||||||
chr11:108184951
|
T | C | 6 | a0002c0002t0002g0020a0002c0002t0002g0264a0002c0002t0002g0265others(3): Show | 7 | HG01074.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+281A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184951 | ||||||
chr11:108184958
|
T | C | 11 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+274A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108184958 | ||||||
chr11:108185009
|
T | C | 27 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(24): Show | 28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.906+223A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185009 | ||||||
chr11:108185086
|
T | A | 1 | a0002c0002t0002g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.906+146A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185086 | ||||||
chr11:108185102
|
C | A | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+130G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185102 | ||||||
chr11:108185202
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.906+30G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 10/17 | chr11 | 108185202 | ||||||
chr11:108185350
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.819-31A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 9/17 | chr11 | 108185350 | ||||||
chr11:108185753
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727-259A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185753 | ||||||
chr11:108185763
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.727-269G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185763 | ||||||
chr11:108185764
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-270A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185764 | ||||||
chr11:108185784
|
A | C | 3 | a0001c0001t0002g0199a0015c0018t0002g0198a0018c0014t0002g0197 | 3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.727-290T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185784 | ||||||
chr11:108185799
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727-305G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185799 | ||||||
chr11:108185981
|
A | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.727-487T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108185981 | ||||||
chr11:108186171
|
C | A | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.726+311G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108186171 | ||||||
chr11:108186205
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.726+277C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108186205 | ||||||
chr11:108186242
|
C | T | 1 | a0001c0006t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.726+240G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 8/17 | chr11 | 108186242 | ||||||
chr11:108186578
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.639-9G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186578 | ||||||
chr11:108186658
|
A | G | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.639-89T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186658 | ||||||
chr11:108186690
|
T | C | 1 | a0002c0002t0002g0019 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.639-121A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186690 | ||||||
chr11:108186703
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(142): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.639-134C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108186703 | ||||||
chr11:108187096
|
A | C | 1 | a0002c0002t0002g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.639-527T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187096 | ||||||
chr11:108187129
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.639-560C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187129 | ||||||
chr11:108187191
|
C | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(96): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.639-622G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187191 | ||||||
chr11:108187304
|
T | C | 1 | a0002c0002t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.639-735A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187304 | ||||||
chr11:108187385
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.638+713C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187385 | ||||||
chr11:108187662
|
C | CACACTTT others(22): Show |
4 | a0001c0001t0002g0179a0002c0002t0004g0215a0002c0002t0004g0216others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+435_638+436ins others(29): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187662 | ||||||
chr11:108187662
|
C | CACACTTT others(51): Show |
2 | a0001c0001t0009g0178a0019c0012t0004g0218 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.638+435_638+436ins others(58): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187662 | ||||||
chr11:108187686
|
G | A | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(314): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.638+412C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187686 | ||||||
chr11:108187818
|
C | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+280G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187818 | ||||||
chr11:108187836
|
T | C | 5 | a0001c0001t0001g0081a0001c0001t0001g0135a0001c0001t0001g0175others(2): Show | 5 | HG00423.hp2 NA18944.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+262A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187836 | ||||||
chr11:108187908
|
T | C | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02132.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+190A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108187908 | ||||||
chr11:108188042
|
CT | C | 7 | a0001c0001t0001g0120a0001c0001t0001g0131a0001c0001t0002g0296others(4): Show | 7 | HG01515.hp1 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+55delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108188042 | ||||||
chr11:108188067
|
G | A | 6 | a0001c0001t0002g0163a0002c0002t0007g0026a0004c0004t0002g0302others(3): Show | 6 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.638+31C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 7/17 | chr11 | 108188067 | ||||||
chr11:108188273
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(142): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.557-94A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188273 | ||||||
chr11:108188323
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.557-144A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188323 | ||||||
chr11:108188509
|
C | T | 1 | a0003c0003t0002g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.557-330G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188509 | ||||||
chr11:108188602
|
C | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0032others(1): Show | 5 | HG01123.hp1 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-423G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188602 | ||||||
chr11:108188778
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.556+328G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188778 | ||||||
chr11:108188842
|
T | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.556+264A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188842 | ||||||
chr11:108188893
|
A | G | 1 | a0003c0003t0002g0247 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.556+213T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188893 | ||||||
chr11:108188973
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.556+133G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188973 | ||||||
chr11:108188975
|
A | G | 1 | a0002c0002t0002g0268 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.556+131T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108188975 | ||||||
chr11:108189008
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.556+98G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 6/17 | chr11 | 108189008 | ||||||
chr11:108189397
|
A | G | 1 | a0003c0003t0002g0247 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.332-67T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189397 | ||||||
chr11:108189478
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0152 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.332-148G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189478 | ||||||
chr11:108189557
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(8): Show | 13 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-227A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189557 | ||||||
chr11:108189596
|
C | T | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-266G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189596 | ||||||
chr11:108189597
|
G | A | 35 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(32): Show | 36 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-267C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189597 | ||||||
chr11:108189609
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.332-279C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189609 | ||||||
chr11:108189645
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332-315G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189645 | ||||||
chr11:108189646
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0002g0199a0001c0001t0002g0200others(2): Show | 5 | HG00140.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-316C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189646 | ||||||
chr11:108189652
|
C | T | 3 | a0001c0001t0001g0167a0002c0022t0002g0315a0004c0004t0002g0310 | 3 | HG02451.hp1 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.332-322G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189652 | ||||||
chr11:108189686
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.332-356G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189686 | ||||||
chr11:108189742
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0112 | 3 | NA18979.hp2 NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.332-412G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189742 | ||||||
chr11:108189795
|
G | C | 1 | a0006c0007t0001g0104 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.332-465C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189795 | ||||||
chr11:108189836
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.332-506G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189836 | ||||||
chr11:108189869
|
C | CA | 33 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0058others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.332-540dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189869 | ||||||
chr11:108189885
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0164a0001c0001t0001g0168others(6): Show | 11 | HG02602.hp2 HG03688.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.332-555G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108189885 | ||||||
chr11:108190010
|
A | T | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+450T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190010 | ||||||
chr11:108190086
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.331+374G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190086 | ||||||
chr11:108190295
|
A | G | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.331+165T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190295 | ||||||
chr11:108190300
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.331+160C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190300 | ||||||
chr11:108190312
|
CA | C | 105 | a0001c0001t0001g0085a0001c0001t0001g0141a0001c0001t0001g0142others(102): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.331+147delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | ||||||
chr11:108190312
|
CAA | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 70 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.331+146_331+147del others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | ||||||
chr11:108190312
|
CAAA | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(115): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.331+145_331+147del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | ||||||
chr11:108190312
|
CAAAA | C | 16 | a0001c0001t0001g0044a0001c0001t0001g0120a0001c0001t0001g0126others(13): Show | 17 | HG01070.hp2 HG01243.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.331+144_331+147del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 5/17 | chr11 | 108190312 | ||||||
chr11:108190518
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02132.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-18C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190518 | ||||||
chr11:108190562
|
TTTAG | T | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-66_291-63delCT others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190562 | ||||||
chr11:108190652
|
C | T | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(312): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.291-152G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190652 | ||||||
chr11:108190699
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0147 | 2 | NA18964.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.291-199G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190699 | ||||||
chr11:108190850
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.291-350T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108190850 | ||||||
chr11:108191081
|
C | A | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.291-581G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191081 | ||||||
chr11:108191391
|
C | T | 1 | a0003c0003t0002g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.290+727G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191391 | ||||||
chr11:108191582
|
T | G | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.290+536A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191582 | ||||||
chr11:108191600
|
T | C | 2 | a0002c0002t0006g0242a0002c0002t0006g0279 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.290+518A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191600 | ||||||
chr11:108191659
|
T | C | 1 | a0002c0002t0002g0024 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.290+459A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191659 | ||||||
chr11:108191814
|
G | GAATT | 3 | a0003c0003t0002g0022a0003c0003t0002g0246a0003c0003t0002g0262 | 4 | HG00733.hp2 HG00735.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+300_290+303dup others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108191814 | ||||||
chr11:108192029
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+89T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 4/17 | chr11 | 108192029 | ||||||
chr11:108192199
|
T | C | 2 | a0002c0002t0002g0220a0002c0002t0007g0026 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.218-9A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192199 | ||||||
chr11:108192289
|
T | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.218-99A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192289 | ||||||
chr11:108192424
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-234A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192424 | ||||||
chr11:108192611
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02132.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-421G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192611 | ||||||
chr11:108192659
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.218-469T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192659 | ||||||
chr11:108192718
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.218-528C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192718 | ||||||
chr11:108192803
|
T | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.218-613A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192803 | ||||||
chr11:108192823
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.218-633C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192823 | ||||||
chr11:108192961
|
AAAAC | A | 13 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-775_218-772del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108192961 | ||||||
chr11:108193001
|
T | C | 1 | a0002c0002t0002g0259 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.218-811A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193001 | ||||||
chr11:108193047
|
G | A | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.218-857C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193047 | ||||||
chr11:108193167
|
C | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0121 | 2 | HG01175.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.217+790G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193167 | ||||||
chr11:108193170
|
A | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0121 | 2 | HG01175.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.217+787T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193170 | ||||||
chr11:108193658
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+299C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193658 | ||||||
chr11:108193693
|
C | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.217+264G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193693 | ||||||
chr11:108193880
|
T | C | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+77A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193880 | ||||||
chr11:108193918
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+39C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 3/17 | chr11 | 108193918 | ||||||
chr11:108194034
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157-17G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194034 | ||||||
chr11:108194083
|
A | G | 2 | a0003c0003t0002g0255a0003c0003t0002g0281 | 2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.157-66T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194083 | ||||||
chr11:108194208
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(138): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-191T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194208 | ||||||
chr11:108194235
|
T | C | 1 | a0002c0002t0002g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.157-218A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194235 | ||||||
chr11:108194525
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(8): Show | 13 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-508T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194525 | ||||||
chr11:108194632
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-615C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194632 | ||||||
chr11:108194825
|
AT | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0120others(7): Show | 12 | HG00558.hp2 HG00639.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-809delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194825 | ||||||
chr11:108194889
|
T | C | 1 | a0002c0002t0002g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.157-872A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194889 | ||||||
chr11:108194893
|
G | A | 2 | a0001c0001t0002g0190a0004c0004t0002g0189 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.157-876C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194893 | ||||||
chr11:108194944
|
C | T | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.157-927G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194944 | ||||||
chr11:108194948
|
C | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-931G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194948 | ||||||
chr11:108194981
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.157-964C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194981 | ||||||
chr11:108194999
|
T | G | 4 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-982A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108194999 | ||||||
chr11:108195061
|
A | C | 3 | a0002c0002t0002g0256a0002c0002t0002g0257a0002c0002t0002g0259 | 3 | HG01496.hp2 HG02523.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.157-1044T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195061 | ||||||
chr11:108195289
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.157-1272A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195289 | ||||||
chr11:108195333
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.157-1316G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195333 | ||||||
chr11:108195403
|
A | T | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.157-1386T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195403 | ||||||
chr11:108195614
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-1597T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195614 | ||||||
chr11:108195635
|
CT | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.157-1619delA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195635 | ||||||
chr11:108195761
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1541C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195761 | ||||||
chr11:108195983
|
T | G | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.156+1319A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108195983 | ||||||
chr11:108196004
|
C | T | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1298G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196004 | ||||||
chr11:108196024
|
G | T | 1 | a0002c0002t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156+1278C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196024 | ||||||
chr11:108196096
|
T | C | 3 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.156+1206A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196096 | ||||||
chr11:108196193
|
G | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.156+1109C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196193 | ||||||
chr11:108196283
|
T | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1019A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196283 | ||||||
chr11:108196507
|
ATAAT | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.156+791_156+794del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196507 | ||||||
chr11:108196670
|
T | C | 1 | a0005c0005t0001g0011 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.156+632A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196670 | ||||||
chr11:108196732
|
T | G | 1 | a0001c0001t0002g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.156+570A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196732 | ||||||
chr11:108196863
|
A | G | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.156+439T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196863 | ||||||
chr11:108196871
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.156+431A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196871 | ||||||
chr11:108196893
|
A | G | 1 | a0001c0001t0003g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.156+409T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196893 | ||||||
chr11:108196998
|
G | A | 11 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+304C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 2/17 | chr11 | 108196998 | ||||||
chr11:108197665
|
A | G | 1 | a0004c0004t0002g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.38-245T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108197665 | ||||||
chr11:108198057
|
T | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-637A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198057 | ||||||
chr11:108198227
|
T | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.38-807A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198227 | ||||||
chr11:108198312
|
T | C | 2 | a0002c0002t0002g0192a0002c0002t0002g0295 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.38-892A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198312 | ||||||
chr11:108198347
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.38-927C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198347 | ||||||
chr11:108198424
|
G | A | 1 | a0004c0004t0002g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.38-1004C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198424 | ||||||
chr11:108198512
|
C | CAG | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.38-1093_38-1092ins others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198512 | ||||||
chr11:108198669
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.38-1249A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198669 | ||||||
chr11:108198877
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.38-1457T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198877 | ||||||
chr11:108198909
|
T | A | 13 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.38-1489A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108198909 | ||||||
chr11:108199020
|
G | C | 1 | a0002c0002t0002g0024 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.38-1600C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199020 | ||||||
chr11:108199092
|
C | T | 1 | a0009c0024t0002g0225 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.38-1672G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199092 | ||||||
chr11:108199232
|
G | A | 2 | a0003c0003t0002g0212a0003c0003t0002g0214 | 2 | NA18946.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.38-1812C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199232 | ||||||
chr11:108199234
|
G | A | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-1814C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199234 | ||||||
chr11:108199403
|
C | T | 1 | a0004c0004t0002g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.38-1983G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199403 | ||||||
chr11:108199578
|
C | T | 1 | a0001c0001t0003g0123 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.38-2158G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199578 | ||||||
chr11:108199583
|
G | A | 2 | a0002c0002t0002g0220a0002c0002t0007g0026 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-2163C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199583 | ||||||
chr11:108199595
|
C | G | 2 | a0002c0002t0002g0220a0002c0002t0007g0026 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-2175G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199595 | ||||||
chr11:108199846
|
C | T | 4 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-2426G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108199846 | ||||||
chr11:108200206
|
G | A | 1 | a0002c0002t0007g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.38-2786C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200206 | ||||||
chr11:108200222
|
G | C | 3 | a0004c0004t0002g0304a0004c0004t0002g0305a0004c0004t0002g0306 | 3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.38-2802C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200222 | ||||||
chr11:108200438
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.38-3018G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200438 | ||||||
chr11:108200439
|
G | A | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.38-3019C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200439 | ||||||
chr11:108200523
|
C | T | 3 | a0001c0001t0002g0199a0015c0018t0002g0198a0018c0014t0002g0197 | 3 | HG00140.hp2 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.38-3103G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200523 | ||||||
chr11:108200539
|
T | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-3119A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200539 | ||||||
chr11:108200694
|
A | G | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.38-3274T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200694 | ||||||
chr11:108200755
|
C | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-3335G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200755 | ||||||
chr11:108200855
|
T | G | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-3435A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108200855 | ||||||
chr11:108201517
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-4097C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201517 | ||||||
chr11:108201545
|
C | T | 4 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-4125G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201545 | ||||||
chr11:108201705
|
G | A | 1 | a0002c0002t0002g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.38-4285C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201705 | ||||||
chr11:108201781
|
G | T | 3 | a0003c0003t0002g0284a0003c0003t0002g0285a0003c0003t0002g0288 | 3 | NA18955.hp1 NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.38-4361C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201781 | ||||||
chr11:108201875
|
T | G | 1 | a0002c0002t0002g0263 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.38-4455A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108201875 | ||||||
chr11:108202001
|
C | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 17 | HG00558.hp2 HG00639.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.38-4581G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202001 | ||||||
chr11:108202085
|
T | C | 1 | a0003c0003t0002g0288 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.38-4665A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202085 | ||||||
chr11:108202345
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-4925C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202345 | ||||||
chr11:108202385
|
C | G | 1 | a0002c0002t0002g0314 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.38-4965G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202385 | ||||||
chr11:108202448
|
G | T | 1 | a0019c0012t0004g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.38-5028C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202448 | ||||||
chr11:108202569
|
C | A | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-5149G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202569 | ||||||
chr11:108202659
|
T | C | 8 | a0002c0002t0002g0020a0002c0002t0002g0221a0002c0002t0002g0264others(5): Show | 9 | HG01074.hp2 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-5239A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202659 | ||||||
chr11:108202887
|
T | G | 1 | a0003c0003t0002g0280 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.38-5467A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108202887 | ||||||
chr11:108203239
|
A | G | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-5819T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203239 | ||||||
chr11:108203342
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-5922G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203342 | ||||||
chr11:108203464
|
A | G | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-6044T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203464 | ||||||
chr11:108203477
|
G | A | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-6057C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203477 | ||||||
chr11:108203521
|
G | T | 1 | a0003c0003t0002g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.38-6101C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203521 | ||||||
chr11:108203540
|
C | A | 1 | a0002c0002t0002g0274 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.38-6120G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203540 | ||||||
chr11:108203603
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.38-6183A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203603 | ||||||
chr11:108203605
|
A | G | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(314): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.38-6185T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203605 | ||||||
chr11:108203620
|
G | A | 1 | a0001c0001t0003g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.38-6200C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203620 | ||||||
chr11:108203726
|
CAGTT | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-6310_38-6307del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203726 | ||||||
chr11:108203870
|
T | C | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-6450A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108203870 | ||||||
chr11:108204153
|
C | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-6733G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204153 | ||||||
chr11:108204175
|
C | G | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-6755G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204175 | ||||||
chr11:108204212
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.38-6792T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204212 | ||||||
chr11:108204380
|
T | TG | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.38-6961dupC | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204380 | ||||||
chr11:108204434
|
A | C | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.38-7014T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204434 | ||||||
chr11:108204458
|
T | C | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-7038A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204458 | ||||||
chr11:108204544
|
GGAACCTG others(2): Show |
G | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.38-7133_38-7125del others(9): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204544 | ||||||
chr11:108204571
|
A | C | 1 | a0002c0002t0002g0258 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.38-7151T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204571 | ||||||
chr11:108204608
|
C | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-7188G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204608 | ||||||
chr11:108204639
|
G | A | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-7219C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204639 | ||||||
chr11:108204963
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0049 | 3 | NA18966.hp1 NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.38-7543C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108204963 | ||||||
chr11:108205185
|
T | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.38-7765A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205185 | ||||||
chr11:108205479
|
A | C | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-8059T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205479 | ||||||
chr11:108205505
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.38-8085G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205505 | ||||||
chr11:108205610
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.38-8190G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205610 | ||||||
chr11:108205732
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.38-8312A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205732 | ||||||
chr11:108205913
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.38-8493C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205913 | ||||||
chr11:108205985
|
C | G | 1 | a0014c0017t0002g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.38-8565G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108205985 | ||||||
chr11:108206052
|
C | A | 2 | a0003c0003t0002g0255a0003c0003t0002g0281 | 2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.38-8632G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206052 | ||||||
chr11:108206275
|
TTGCC | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-8859_38-8856del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206275 | ||||||
chr11:108206311
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.38-8891G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206311 | ||||||
chr11:108206330
|
G | A | 2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.38-8910C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206330 | ||||||
chr11:108206425
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.38-9005G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206425 | ||||||
chr11:108206454
|
A | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.38-9034T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206454 | ||||||
chr11:108206467
|
C | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-9047G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206467 | ||||||
chr11:108206732
|
G | A | 2 | a0002c0002t0002g0194a0002c0002t0002g0195 | 2 | HG01081.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.38-9312C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206732 | ||||||
chr11:108206809
|
C | T | 1 | a0002c0002t0002g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.38-9389G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108206809 | ||||||
chr11:108207035
|
A | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0049 | 3 | NA18966.hp1 NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.38-9615T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207035 | ||||||
chr11:108207129
|
C | T | 1 | a0002c0002t0002g0274 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.38-9709G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207129 | ||||||
chr11:108207130
|
G | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.38-9710C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207130 | ||||||
chr11:108207156
|
G | C | 27 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(24): Show | 28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.38-9736C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207156 | ||||||
chr11:108207238
|
G | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-9818C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207238 | ||||||
chr11:108207542
|
G | C | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-10122C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207542 | ||||||
chr11:108207596
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.38-10176G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207596 | ||||||
chr11:108207616
|
C | G | 3 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.38-10196G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207616 | ||||||
chr11:108207652
|
G | A | 7 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0183others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-10232C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207652 | ||||||
chr11:108207663
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0005g0039a0001c0001t0005g0040 | 4 | HG01255.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-10243G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207663 | ||||||
chr11:108207684
|
C | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-10264G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207684 | ||||||
chr11:108207720
|
G | C | 3 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.38-10300C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207720 | ||||||
chr11:108207966
|
G | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.38-10546C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108207966 | ||||||
chr11:108208233
|
A | G | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-10813T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208233 | ||||||
chr11:108208483
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.38-11063C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208483 | ||||||
chr11:108208532
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02132.hp2 HG03579.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-11112C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208532 | ||||||
chr11:108208542
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.38-11122A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208542 | ||||||
chr11:108208544
|
C | T | 1 | a0016c0019t0002g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.38-11124G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208544 | ||||||
chr11:108208588
|
T | TA | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.38-11169dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208588 | ||||||
chr11:108208603
|
A | C | 1 | a0002c0002t0002g0023 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.38-11183T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208603 | ||||||
chr11:108208821
|
A | G | 1 | a0002c0002t0002g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.38-11401T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208821 | ||||||
chr11:108208886
|
G | C | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-11466C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108208886 | ||||||
chr11:108209000
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-11580G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209000 | ||||||
chr11:108209026
|
T | G | 1 | a0001c0001t0003g0114 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.38-11606A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209026 | ||||||
chr11:108209288
|
A | G | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38-11868T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209288 | ||||||
chr11:108209298
|
A | T | 1 | a0001c0001t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.38-11878T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209298 | ||||||
chr11:108209366
|
C | T | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.38-11946G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209366 | ||||||
chr11:108209381
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.38-11961C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209381 | ||||||
chr11:108209401
|
T | C | 1 | a0005c0005t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.38-11981A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209401 | ||||||
chr11:108209418
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.38-11998T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209418 | ||||||
chr11:108209462
|
T | C | 2 | a0002c0002t0002g0205a0002c0002t0002g0206 | 2 | NA18979.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.38-12042A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209462 | ||||||
chr11:108209637
|
C | T | 1 | a0002c0002t0002g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.38-12217G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209637 | ||||||
chr11:108209672
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.38-12252C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209672 | ||||||
chr11:108209685
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(141): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.38-12265G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209685 | ||||||
chr11:108209705
|
T | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.38-12285A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209705 | ||||||
chr11:108209837
|
G | A | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.38-12417C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209837 | ||||||
chr11:108209856
|
T | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.38-12436A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209856 | ||||||
chr11:108209888
|
C | CA | 6 | a0001c0001t0002g0163a0002c0002t0002g0193a0002c0002t0002g0268others(3): Show | 6 | HG01175.hp2 HG01346.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-12469dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | ||||||
chr11:108209888
|
CA | C | 101 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(98): Show | 108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.38-12469delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | ||||||
chr11:108209888
|
CAA | C | 16 | a0002c0002t0002g0224a0002c0002t0002g0270a0003c0003t0002g0208others(13): Show | 17 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-12470_38-12469d others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | ||||||
chr11:108209888
|
CAAAAA | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(20): Show | 27 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.38-12473_38-12469d others(7): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | ||||||
chr11:108209888
|
CAAAAAA | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.38-12474_38-12469d others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209888 | ||||||
chr11:108209940
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.38-12520C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108209940 | ||||||
chr11:108210419
|
C | T | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+12081G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210419 | ||||||
chr11:108210476
|
T | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+12024A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210476 | ||||||
chr11:108210696
|
A | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+11804T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210696 | ||||||
chr11:108210731
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+11769G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210731 | ||||||
chr11:108210903
|
C | T | 1 | a0004c0004t0002g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.37+11597G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108210903 | ||||||
chr11:108211036
|
T | C | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+11464A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211036 | ||||||
chr11:108211130
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0009g0178 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+11370G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211130 | ||||||
chr11:108211132
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.37+11368G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211132 | ||||||
chr11:108211159
|
T | C | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+11341A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211159 | ||||||
chr11:108211170
|
C | T | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+11330G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211170 | ||||||
chr11:108211172
|
C | T | 1 | a0002c0002t0002g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.37+11328G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211172 | ||||||
chr11:108211307
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.37+11193G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211307 | ||||||
chr11:108211362
|
CA | C | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(314): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.37+11137delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211362 | ||||||
chr11:108211453
|
G | A | 27 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(24): Show | 28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+11047C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211453 | ||||||
chr11:108211546
|
G | GA | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 43 | HG00438.hp2 HG00741.hp1 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.37+10953dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211546 | ||||||
chr11:108211546
|
GA | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0065others(8): Show | 12 | HG00673.hp1 HG01934.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+10953delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211546 | ||||||
chr11:108211623
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.37+10877C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108211623 | ||||||
chr11:108212036
|
A | G | 1 | a0003c0003t0002g0222 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.37+10464T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212036 | ||||||
chr11:108212046
|
A | C | 1 | a0002c0022t0002g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37+10454T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212046 | ||||||
chr11:108212074
|
TA | T | 14 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0141others(11): Show | 14 | HG01081.hp1 HG01099.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.37+10425delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212074 | ||||||
chr11:108212134
|
A | G | 3 | a0002c0002t0004g0215a0002c0002t0004g0216a0002c0002t0004g0217 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.37+10366T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212134 | ||||||
chr11:108212135
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 6 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+10365A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212135 | ||||||
chr11:108212170
|
T | C | 1 | a0002c0002t0002g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.37+10330A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212170 | ||||||
chr11:108212291
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.37+10209C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212291 | ||||||
chr11:108212399
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.37+10101G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212399 | ||||||
chr11:108212422
|
G | A | 1 | a0011c0023t0003g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.37+10078C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212422 | ||||||
chr11:108212449
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.37+10051G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212449 | ||||||
chr11:108212604
|
T | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0028others(30): Show | 34 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.37+9896A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212604 | ||||||
chr11:108212647
|
C | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0029others(6): Show | 11 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.37+9853G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212647 | ||||||
chr11:108212945
|
C | CA | 23 | a0001c0001t0001g0047a0001c0001t0001g0122a0001c0001t0002g0296others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.37+9554dupT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | ||||||
chr11:108212945
|
CA | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.37+9554delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | ||||||
chr11:108212945
|
CAA | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0149a0001c0001t0001g0150others(10): Show | 13 | HG00140.hp2 HG01081.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.37+9553_37+9554del others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | ||||||
chr11:108212945
|
CAAAA | C | 8 | a0001c0001t0002g0163a0003c0003t0002g0211a0003c0003t0002g0212others(5): Show | 8 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+9551_37+9554del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212945 | ||||||
chr11:108212995
|
C | T | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+9505G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108212995 | ||||||
chr11:108213053
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.37+9447G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213053 | ||||||
chr11:108213188
|
G | A | 8 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(5): Show | 8 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+9312C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213188 | ||||||
chr11:108213256
|
A | C | 1 | a0003c0003t0002g0210 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.37+9244T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213256 | ||||||
chr11:108213363
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0169 | 2 | NA18970.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.37+9137T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213363 | ||||||
chr11:108213413
|
A | G | 1 | a0001c0001t0008g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.37+9087T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213413 | ||||||
chr11:108213487
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 22 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.37+9013G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213487 | ||||||
chr11:108213519
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+8981G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213519 | ||||||
chr11:108213520
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.37+8980C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213520 | ||||||
chr11:108213675
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.37+8825G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213675 | ||||||
chr11:108213734
|
A | G | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+8766T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213734 | ||||||
chr11:108213786
|
G | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.37+8714C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213786 | ||||||
chr11:108213800
|
A | G | 1 | a0002c0002t0007g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37+8700T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213800 | ||||||
chr11:108213842
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.37+8658A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108213842 | ||||||
chr11:108214008
|
C | G | 1 | a0002c0002t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.37+8492G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214008 | ||||||
chr11:108214021
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.37+8479T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214021 | ||||||
chr11:108214338
|
A | G | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+8162T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214338 | ||||||
chr11:108214357
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0126others(14): Show | 18 | HG00438.hp2 HG02135.hp2 NA18941.hp1 others(15): Show |
intron_variant | MODIFIER | c.37+8143C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214357 | ||||||
chr11:108214377
|
T | C | 1 | a0002c0002t0002g0019 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.37+8123A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214377 | ||||||
chr11:108214397
|
C | T | 1 | a0002c0002t0002g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.37+8103G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214397 | ||||||
chr11:108214599
|
G | A | 1 | a0002c0002t0007g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37+7901C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214599 | ||||||
chr11:108214631
|
A | AT | 12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 13 | HG01175.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.37+7868dupA | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214631 | ||||||
chr11:108214658
|
G | A | 1 | a0002c0002t0010g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.37+7842C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214658 | ||||||
chr11:108214665
|
T | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+7835A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214665 | ||||||
chr11:108214691
|
G | C | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+7809C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214691 | ||||||
chr11:108214789
|
T | C | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+7711A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214789 | ||||||
chr11:108214958
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37+7542C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214958 | ||||||
chr11:108214958
|
G | T | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+7542C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214958 | ||||||
chr11:108214983
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.37+7517G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108214983 | ||||||
chr11:108215029
|
C | A | 1 | a0003c0003t0002g0283 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.37+7471G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215029 | ||||||
chr11:108215035
|
T | G | 1 | a0002c0002t0007g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37+7465A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215035 | ||||||
chr11:108215081
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(10): Show | 15 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.37+7419A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215081 | ||||||
chr11:108215098
|
T | C | 6 | a0003c0003t0002g0201a0003c0003t0002g0284a0003c0003t0002g0285others(3): Show | 6 | HG02129.hp1 NA18955.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+7402A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215098 | ||||||
chr11:108215107
|
G | A | 3 | a0001c0001t0002g0163a0014c0017t0002g0162a0016c0019t0002g0161 | 3 | HG02257.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.37+7393C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215107 | ||||||
chr11:108215228
|
C | G | 2 | a0001c0001t0002g0190a0004c0004t0002g0189 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.37+7272G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215228 | ||||||
chr11:108215274
|
TAGTC | T | 5 | a0001c0001t0002g0163a0003c0003t0002g0207a0012c0013t0002g0160others(2): Show | 5 | HG00741.hp1 HG01175.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+7222_37+7225del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215274 | ||||||
chr11:108215342
|
A | G | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+7158T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215342 | ||||||
chr11:108215506
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+6994T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215506 | ||||||
chr11:108215528
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+6972A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215528 | ||||||
chr11:108215715
|
C | T | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+6785G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215715 | ||||||
chr11:108215720
|
T | C | 1 | a0002c0002t0002g0289 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.37+6780A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215720 | ||||||
chr11:108215761
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.37+6739T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215761 | ||||||
chr11:108215852
|
T | A | 1 | a0002c0002t0002g0196 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.37+6648A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215852 | ||||||
chr11:108215875
|
T | C | 4 | a0002c0002t0002g0024a0002c0002t0002g0290a0002c0002t0002g0291others(1): Show | 5 | HG00738.hp2 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+6625A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108215875 | ||||||
chr11:108216079
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+6421G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216079 | ||||||
chr11:108216085
|
T | A | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+6415A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216085 | ||||||
chr11:108216094
|
T | TAAAAAAA others(1): Show |
13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+6405_37+6406ins others(8): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216094 | ||||||
chr11:108216095
|
C | A | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+6405G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216095 | ||||||
chr11:108216150
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.37+6350A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216150 | ||||||
chr11:108216253
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.37+6247A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216253 | ||||||
chr11:108216336
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+6164G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216336 | ||||||
chr11:108216477
|
A | G | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+6023T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216477 | ||||||
chr11:108216491
|
T | C | 1 | a0002c0002t0004g0316 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+6009A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216491 | ||||||
chr11:108216514
|
CA | C | 4 | a0002c0002t0002g0203a0002c0002t0002g0204a0002c0002t0002g0205others(1): Show | 4 | NA18942.hp2 NA18979.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+5985delT | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216514 | ||||||
chr11:108216586
|
C | T | 1 | a0005c0005t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.37+5914G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216586 | ||||||
chr11:108216654
|
T | TGGAAA | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.37+5845_37+5846ins others(5): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216654 | ||||||
chr11:108216827
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.37+5673G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216827 | ||||||
chr11:108216896
|
A | T | 27 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(24): Show | 28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+5604T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108216896 | ||||||
chr11:108217109
|
C | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18962.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.37+5391G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217109 | ||||||
chr11:108217110
|
A | G | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+5390T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217110 | ||||||
chr11:108217120
|
G | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(111): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.37+5380C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217120 | ||||||
chr11:108217167
|
ATGAG | A | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+5329_37+5332del others(4): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217167 | ||||||
chr11:108217428
|
A | C | 1 | a0002c0020t0002g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.37+5072T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217428 | ||||||
chr11:108217758
|
C | T | 27 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(24): Show | 28 | HG01070.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+4742G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217758 | ||||||
chr11:108217766
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.37+4734T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108217766 | ||||||
chr11:108218068
|
T | C | 1 | a0001c0001t0001g0016 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.37+4432A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218068 | ||||||
chr11:108218173
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.37+4327G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218173 | ||||||
chr11:108218313
|
T | A | 4 | a0001c0006t0001g0050a0001c0006t0001g0051a0001c0006t0001g0053others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+4187A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218313 | ||||||
chr11:108218364
|
TAA | T | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0015c0018t0002g0198others(1): Show | 4 | HG00140.hp2 HG02818.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+4134_37+4135del others(2): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218364 | ||||||
chr11:108218404
|
C | T | 1 | a0003c0003t0002g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.37+4096G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218404 | ||||||
chr11:108218406
|
C | T | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+4094G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218406 | ||||||
chr11:108218424
|
T | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.37+4076A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218424 | ||||||
chr11:108218433
|
TTTA | T | 8 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(5): Show | 8 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+4064_37+4066del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218433 | ||||||
chr11:108218470
|
G | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.37+4030C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218470 | ||||||
chr11:108218478
|
T | C | 2 | a0008c0009t0002g0293a0008c0009t0002g0294 | 2 | HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.37+4022A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218478 | ||||||
chr11:108218524
|
T | C | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+3976A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218524 | ||||||
chr11:108218595
|
A | G | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+3905T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218595 | ||||||
chr11:108218700
|
T | C | 1 | a0001c0006t0001g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.37+3800A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218700 | ||||||
chr11:108218714
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.37+3786C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108218714 | ||||||
chr11:108219194
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.37+3306C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219194 | ||||||
chr11:108219282
|
C | G | 1 | a0004c0004t0002g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.37+3218G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219282 | ||||||
chr11:108219335
|
C | G | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+3165G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219335 | ||||||
chr11:108219346
|
C | A | 4 | a0001c0001t0002g0163a0012c0013t0002g0160a0014c0017t0002g0162others(1): Show | 4 | HG01175.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+3154G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219346 | ||||||
chr11:108219380
|
T | TG | 4 | a0001c0006t0001g0050a0001c0006t0001g0051a0001c0006t0001g0053others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+3119dupC | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219380 | ||||||
chr11:108219592
|
C | T | 1 | a0002c0002t0002g0196 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.37+2908G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219592 | ||||||
chr11:108219608
|
T | C | 2 | a0002c0002t0002g0192a0002c0002t0002g0295 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.37+2892A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219608 | ||||||
chr11:108219669
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(13): Show | 19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.37+2831A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219669 | ||||||
chr11:108219732
|
A | AAAC | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 28 | HG01081.hp1 HG01123.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+2765_37+2767dup others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219732 | ||||||
chr11:108219732
|
AAAC | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(147): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.37+2765_37+2767del others(3): Show |
NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219732 | ||||||
chr11:108219961
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37+2539A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219961 | ||||||
chr11:108219983
|
A | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.37+2517T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108219983 | ||||||
chr11:108220304
|
T | C | 13 | a0004c0004t0002g0025a0004c0004t0002g0299a0004c0004t0002g0300others(10): Show | 14 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.37+2196A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220304 | ||||||
chr11:108220378
|
A | C | 1 | a0001c0001t0001g0009 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.37+2122T>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220378 | ||||||
chr11:108220441
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.37+2059A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220441 | ||||||
chr11:108220442
|
A | T | 1 | a0002c0002t0002g0192 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37+2058T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220442 | ||||||
chr11:108220450
|
C | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG01123.hp1 HG02109.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+2050G>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220450 | ||||||
chr11:108220533
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.37+1967G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220533 | ||||||
chr11:108220596
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.37+1904C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220596 | ||||||
chr11:108220660
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | NA18954.hp1 NA18962.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+1840G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220660 | ||||||
chr11:108220678
|
G | T | 1 | a0002c0002t0002g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.37+1822C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220678 | ||||||
chr11:108220770
|
G | T | 8 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(5): Show | 8 | HG02055.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+1730C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108220770 | ||||||
chr11:108221043
|
G | C | 2 | a0001c0001t0002g0190a0004c0004t0002g0189 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.37+1457C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221043 | ||||||
chr11:108221128
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.37+1372A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221128 | ||||||
chr11:108221216
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.37+1284A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221216 | ||||||
chr11:108221386
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.37+1114G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221386 | ||||||
chr11:108221437
|
T | G | 3 | a0002c0002t0002g0312a0002c0002t0002g0313a0002c0002t0002g0314 | 3 | HG00673.hp2 NA19012.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.37+1063A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221437 | ||||||
chr11:108221576
|
C | G | 1 | a0002c0002t0002g0192 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37+924G>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221576 | ||||||
chr11:108221601
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 8 | NA18939.hp2 NA18953.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+899A>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221601 | ||||||
chr11:108221697
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.37+803C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221697 | ||||||
chr11:108221820
|
A | G | 1 | a0002c0002t0002g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.37+680T>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221820 | ||||||
chr11:108221881
|
T | G | 2 | a0002c0002t0004g0316a0002c0022t0002g0315 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.37+619A>C | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221881 | ||||||
chr11:108221887
|
C | T | 11 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.37+613G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221887 | ||||||
chr11:108221910
|
G | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(13): Show | 19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.37+590C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221910 | ||||||
chr11:108221966
|
T | C | 1 | a0002c0002t0002g0317 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.37+534A>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108221966 | ||||||
chr11:108222275
|
G | C | 1 | a0002c0002t0002g0318 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.37+225C>G | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222275 | ||||||
chr11:108222275
|
G | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0029others(5): Show | 10 | HG01123.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.37+225C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222275 | ||||||
chr11:108222308
|
G | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0009g0178 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.37+192C>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222308 | ||||||
chr11:108222350
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.37+150G>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222350 | ||||||
chr11:108222434
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | NA18944.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.37+66C>T | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222434 | ||||||
chr11:108222481
|
A | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.37+19T>A | NPAT | ENSG00000149308.17 | transcript | ENST00000278612.9 | protein_coding | 1/17 | chr11 | 108222481 |