geneid | 8208 |
---|---|
ensemblid | ENSG00000159259.8 |
hgncid | 1911 |
symbol | CHAF1B |
name | chromatin assembly factor 1 subunit B |
refseq_nuc | NM_005441.3 |
refseq_prot | NP_005432.1 |
ensembl_nuc | ENST00000314103.6 |
ensembl_prot | ENSP00000315700.4 |
mane_status | MANE Select |
chr | chr21 |
start | 36385392 |
end | 36419015 |
strand | + |
ver | v1.2 |
region | chr21:36385392-36419015 |
region5000 | chr21:36380392-36424015 |
regionname0 | CHAF1B_chr21_36385392_36419015 |
regionname5000 | CHAF1B_chr21_36380392_36424015 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 559 | 324 | 83 | 64 | 122 | 8 | 45 | 94 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0002 | 0/0 | 559 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0003 | 0/0 | 559 | 7 | 0 | 4 | 0 | 2 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0004 | 0/0 | 559 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0005 | 0/0 | 559 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1680 | 318 | 79 | 63 | 121 | 8 | 45 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0002 | 0/0 | 1680 | 8 | 6 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0003 | 0/0 | 1680 | 7 | 0 | 4 | 0 | 2 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0004 | 0/0 | 1680 | 4 | 1 | 3 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0005 | 0/0 | 1680 | 4 | 3 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0006 | 0/0 | 1680 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0007 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
c0008 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2787 | 150 | 24 | 46 | 50 | 6 | 24 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0002 | 1/1 | 2787 | 69 | 4 | 3 | 44 | 0 | 16 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0003 | 0/0 | 2788 | 21 | 16 | 4 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0004 | 0/0 | 2787 | 11 | 0 | 0 | 11 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0005 | 0/0 | 2788 | 10 | 5 | 3 | 0 | 2 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0006 | 0/0 | 2788 | 8 | 7 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0007 | 0/0 | 2788 | 7 | 1 | 0 | 6 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0008 | 0/0 | 2786 | 6 | 0 | 4 | 0 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0009 | 0/0 | 2788 | 6 | 6 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0010 | 0/0 | 2789 | 5 | 4 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0011 | 0/0 | 2788 | 4 | 0 | 4 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0012 | 0/0 | 2789 | 3 | 3 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0013 | 0/0 | 2788 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0014 | 0/0 | 2790 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0015 | 0/0 | 2786 | 3 | 1 | 0 | 1 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0016 | 0/0 | 2787 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0017 | 0/0 | 2786 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0018 | 0/0 | 2786 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0019 | 0/0 | 2788 | 2 | 1 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0020 | 0/0 | 2788 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0021 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0022 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0023 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0024 | 0/0 | 2788 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0025 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0026 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0027 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0028 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0029 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0030 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0031 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0032 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0033 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0034 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0035 | 0/0 | 2786 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0036 | 0/0 | 2786 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0037 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0038 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0039 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0040 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0041 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0042 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0043 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0044 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0045 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
t0046 | 0/0 | 2789 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1680 | 318 | 79 | 63 | 121 | 8 | 45 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0005 | 0/0 | 1680 | 4 | 3 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0007 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0008 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0002c0002 | 0/0 | 1680 | 8 | 6 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0003c0003 | 0/0 | 1680 | 7 | 0 | 4 | 0 | 2 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0004c0004 | 0/0 | 1680 | 4 | 1 | 3 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0005c0006 | 0/0 | 1680 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4466 | 142 | 24 | 42 | 49 | 4 | 23 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0002 | 1/1 | 4466 | 69 | 4 | 3 | 44 | 0 | 16 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0003 | 0/0 | 4467 | 16 | 14 | 1 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0004 | 0/0 | 4466 | 11 | 0 | 0 | 11 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0005 | 0/0 | 4467 | 10 | 5 | 3 | 0 | 2 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0006 | 0/0 | 4467 | 5 | 5 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0007 | 0/0 | 4467 | 7 | 1 | 0 | 6 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0008 | 0/0 | 4465 | 6 | 0 | 4 | 0 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0009 | 0/0 | 4467 | 6 | 6 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0010 | 0/0 | 4468 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0011 | 0/0 | 4467 | 4 | 0 | 4 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0014 | 0/0 | 4469 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0015 | 0/0 | 4465 | 3 | 1 | 0 | 1 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0016 | 0/0 | 4466 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0017 | 0/0 | 4465 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0018 | 0/0 | 4465 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0019 | 0/0 | 4467 | 2 | 1 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0020 | 0/0 | 4467 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0021 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0022 | 0/0 | 4465 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0023 | 0/0 | 4469 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0024 | 0/0 | 4467 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0025 | 0/0 | 4465 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0026 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0027 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0028 | 0/0 | 4468 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0030 | 0/0 | 4466 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0031 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0032 | 0/0 | 4466 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0033 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0034 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0035 | 0/0 | 4465 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0036 | 0/0 | 4465 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0037 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0038 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0039 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0040 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0041 | 0/0 | 4466 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0042 | 0/0 | 4466 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0043 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0044 | 0/0 | 4466 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0001t0045 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0005t0006 | 0/0 | 4467 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0005t0029 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0007t0003 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0001c0008t0001 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0002c0002t0010 | 0/0 | 4468 | 4 | 3 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0002c0002t0012 | 0/0 | 4468 | 3 | 3 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0002c0002t0046 | 0/0 | 4468 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0003c0003t0001 | 0/0 | 4466 | 7 | 0 | 4 | 0 | 2 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0004c0004t0003 | 0/0 | 4467 | 4 | 1 | 3 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
a0005c0006t0013 | 0/0 | 4467 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | copy fasta | chr21 | 36380392 | 36424015 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0008g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0011g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0011g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0011g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0011g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0014g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0015g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0016g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0016g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0017g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0017g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0018g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0018g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0019g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0019g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0020g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0021g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0022g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0023g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0024g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0025g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0026g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0028g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0030g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0031g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0032g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0033g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0034g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0035g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0036g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0037g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0038g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0039g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0040g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0041g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0042g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0043g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0044g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0001t0045g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0005t0006g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0005t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0005t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0005t0029g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0007t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0001c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0010g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0002c0002t0046g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0004c0004t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0004c0004t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0004c0004t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0004c0004t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0005c0006t0013g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0005c0006t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
a0005c0006t0013g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00323 | hp1 | a0001 | c0001 | t0015 | g0060 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0190 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00408 | hp2 | a0001 | c0001 | t0020 | g0164 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00438 | hp1 | a0001 | c0001 | t0031 | g0254 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00639 | hp2 | a0005 | c0006 | t0013 | g0294 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0055 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0319 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00741 | hp1 | a0001 | c0001 | t0016 | g0202 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01081 | hp1 | a0001 | c0001 | t0042 | g0001 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0191 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01106 | hp1 | a0001 | c0005 | t0006 | g0309 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01109 | hp1 | a0002 | c0002 | t0046 | g0073 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0323 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01167 | hp2 | a0004 | c0004 | t0003 | g0028 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01169 | hp2 | a0004 | c0004 | t0003 | g0029 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01175 | hp1 | a0002 | c0002 | t0010 | g0078 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01175 | hp2 | a0001 | c0001 | t0044 | g0196 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01243 | hp1 | a0004 | c0004 | t0003 | g0033 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0020 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01256 | hp1 | a0001 | c0001 | t0011 | g0015 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01358 | hp1 | a0001 | c0001 | t0011 | g0021 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01358 | hp2 | a0001 | c0001 | t0024 | g0305 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0045 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0312 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0207 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0313 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01884 | hp2 | a0001 | c0001 | t0040 | g0110 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0210 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0324 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0044 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01943 | hp2 | a0001 | c0001 | t0041 | g0185 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01952 | hp2 | a0001 | c0001 | t0014 | g0066 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01978 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0301 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02145 | hp1 | a0002 | c0002 | t0012 | g0075 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0046 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0307 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0043 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02451 | hp1 | a0001 | c0001 | t0015 | g0080 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0048 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02615 | hp1 | a0002 | c0002 | t0010 | g0068 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02622 | hp1 | a0001 | c0001 | t0028 | g0296 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02622 | hp2 | a0001 | c0007 | t0003 | g0076 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02698 | hp2 | a0001 | c0001 | t0020 | g0123 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02717 | hp1 | a0002 | c0002 | t0012 | g0003 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0036 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0300 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0040 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02886 | hp2 | a0001 | c0001 | t0017 | g0302 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0206 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02896 | hp1 | a0001 | c0001 | t0025 | g0052 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02897 | hp2 | a0001 | c0001 | t0026 | g0051 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02922 | hp1 | a0004 | c0004 | t0003 | g0030 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0314 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02970 | hp1 | a0002 | c0002 | t0010 | g0074 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02970 | hp2 | a0001 | c0001 | t0033 | g0203 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02976 | hp1 | a0001 | c0001 | t0034 | g0054 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02976 | hp2 | a0001 | c0001 | t0014 | g0065 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03017 | hp2 | a0001 | c0001 | t0035 | g0327 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0298 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0304 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0306 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03225 | hp1 | a0001 | c0001 | t0016 | g0215 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0072 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0317 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03453 | hp2 | a0001 | c0005 | t0029 | g0308 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03486 | hp1 | a0002 | c0002 | t0012 | g0003 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0042 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03491 | hp1 | a0001 | c0001 | t0032 | g0230 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0287 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03540 | hp1 | a0001 | c0001 | t0038 | g0165 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03654 | hp2 | a0001 | c0001 | t0030 | g0260 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04115 | hp1 | a0001 | c0001 | t0008 | g0047 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18906 | hp1 | a0001 | c0005 | t0006 | g0321 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18940 | hp1 | a0001 | c0001 | t0007 | g0181 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18954 | hp2 | a0001 | c0001 | t0021 | g0118 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18957 | hp2 | a0001 | c0001 | t0036 | g0232 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18959 | hp2 | a0001 | c0001 | t0018 | g0266 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18960 | hp1 | a0001 | c0001 | t0045 | g0208 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18960 | hp2 | a0001 | c0001 | t0019 | g0270 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18963 | hp2 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18965 | hp2 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18969 | hp1 | a0001 | c0001 | t0015 | g0122 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18980 | hp1 | a0001 | c0001 | t0037 | g0186 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18988 | hp1 | a0001 | c0001 | t0043 | g0212 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18993 | hp2 | a0001 | c0008 | t0001 | g0198 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19001 | hp2 | a0001 | c0001 | t0018 | g0063 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19030 | hp2 | a0001 | c0001 | t0023 | g0209 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0194 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0311 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0039 | AFR | ASW | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | TSI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0056 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0067 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02109 | hp2 | a0005 | c0006 | t0013 | g0292 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02486 | hp1 | a0001 | c0005 | t0006 | g0310 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03471 | hp1 | a0001 | c0001 | t0022 | g0328 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG06807 | hp1 | a0005 | c0006 | t0013 | g0293 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA20300 | hp1 | a0001 | c0001 | t0039 | g0189 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
NA21309 | hp2 | a0002 | c0002 | t0010 | g0071 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0231 | REF | REF | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0129 | REF | REF | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36387659
|
C | T | 1 | a0003 | 7 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(4): Show |
missense_variant | MODERATE | c.188C>T | p.Ala63Val | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/14 | 325/4466 | 188/1680 | 63/559 | chr21 | 36387659 | ||
chr21:36413066
|
C | T | 1 | a0005 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.1244C>T | p.Pro415Leu | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/14 | 1381/4466 | 1244/1680 | 415/559 | chr21 | 36413066 | ||
chr21:36415317
|
A | C | 1 | a0002 | 8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
missense_variant | MODERATE | c.1516A>C | p.Lys506Gln | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/14 | 1653/4466 | 1516/1680 | 506/559 | chr21 | 36415317 | ||
chr21:36415321
|
C | T | 1 | a0004 | 4 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(1): Show |
missense_variant | MODERATE | c.1520C>T | p.Thr507Met | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/14 | 1657/4466 | 1520/1680 | 507/559 | chr21 | 36415321 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36402829
|
C | T | 1 | a0001c0008 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.735C>T | p.Asp245Asp | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/14 | 872/4466 | 735/1680 | 245/559 | chr21 | 36402829 | ||
chr21:36413259
|
C | T | 1 | a0001c0005 | 4 | HG01106.hp1 HG02486.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1437C>T | p.His479His | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/14 | 1574/4466 | 1437/1680 | 479/559 | chr21 | 36413259 | ||
chr21:36413280
|
G | A | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1458G>A | p.Leu486Leu | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/14 | 1595/4466 | 1458/1680 | 486/559 | chr21 | 36413280 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36416391
|
C | G | 1 | a0002c0002t0046 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 25 | chr21 | 36416391 | |||||
chr21:36416405
|
G | C | 1 | a0001c0001t0021 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 39 | chr21 | 36416405 | |||||
chr21:36416487
|
A | G | 1 | a0001c0001t0045 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 121 | chr21 | 36416487 | |||||
chr21:36416581
|
C | T | 1 | a0001c0001t0044 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 215 | chr21 | 36416581 | |||||
chr21:36416582
|
G | A | 23 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(20): Show | 76 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 216 | chr21 | 36416582 | |||||
chr21:36416670
|
T | C | 1 | a0001c0001t0022 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 304 | chr21 | 36416670 | |||||
chr21:36416672
|
G | A | 1 | a0001c0001t0030 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 306 | chr21 | 36416672 | |||||
chr21:36416979
|
T | C | 1 | a0002c0002t0012 | 3 | HG02145.hp1 HG02717.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*613T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 613 | chr21 | 36416979 | |||||
chr21:36417024
|
G | T | 5 | a0001c0001t0006a0001c0001t0017a0001c0001t0028others(2): Show | 12 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*658G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 658 | chr21 | 36417024 | |||||
chr21:36417171
|
G | A | 1 | a0001c0001t0023 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*805G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 805 | chr21 | 36417171 | |||||
chr21:36417186
|
C | G | 2 | a0001c0001t0009a0001c0001t0027 | 7 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*820C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 820 | chr21 | 36417186 | |||||
chr21:36417197
|
G | A | 7 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(4): Show | 25 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*831G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 831 | chr21 | 36417197 | |||||
chr21:36417281
|
C | CAT | 2 | a0001c0001t0014a0001c0001t0023 | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*929_*930dupTA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 931 | INFO_REALIGN_3_PRIME | chr21 | 36417281 | ||||
chr21:36417281
|
CAT | C | 2 | a0001c0001t0017a0001c0001t0022 | 3 | HG02886.hp2 HG03209.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*929_*930delTA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 929 | INFO_REALIGN_3_PRIME | chr21 | 36417281 | ||||
chr21:36417320
|
A | G | 2 | a0001c0001t0014a0001c0001t0023 | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*954A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 954 | chr21 | 36417320 | |||||
chr21:36417321
|
T | C | 1 | a0005c0006t0013 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*955T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 955 | chr21 | 36417321 | |||||
chr21:36417330
|
T | A | 24 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(21): Show | 80 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*964T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 964 | chr21 | 36417330 | |||||
chr21:36417461
|
C | T | 1 | a0005c0006t0013 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1095 | chr21 | 36417461 | |||||
chr21:36417486
|
C | G | 1 | a0001c0001t0024 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1120C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1120 | chr21 | 36417486 | |||||
chr21:36417502
|
A | G | 46 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(43): Show | 270 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1136A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1136 | chr21 | 36417502 | |||||
chr21:36417541
|
G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1175 | chr21 | 36417541 | |||||
chr21:36417566
|
A | G | 4 | a0001c0001t0008a0001c0001t0022a0001c0001t0025others(1): Show | 9 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1200A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1200 | chr21 | 36417566 | |||||
chr21:36417591
|
A | G | 2 | a0001c0001t0016a0001c0001t0033 | 4 | HG00741.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1225A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1225 | chr21 | 36417591 | |||||
chr21:36417655
|
G | T | 1 | a0001c0001t0043 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1289G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1289 | chr21 | 36417655 | |||||
chr21:36417747
|
G | A | 1 | a0001c0001t0034 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1381 | chr21 | 36417747 | |||||
chr21:36417833
|
C | T | 1 | a0001c0001t0042 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1467 | chr21 | 36417833 | |||||
chr21:36418017
|
A | AT | 4 | a0001c0001t0007a0001c0001t0019a0001c0001t0026others(1): Show | 11 | HG02622.hp1 HG02897.hp2 HG03098.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1664dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1665 | INFO_REALIGN_3_PRIME | chr21 | 36418017 | ||||
chr21:36418017
|
AT | A | 3 | a0001c0001t0008a0001c0001t0027a0001c0001t0035 | 8 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1664delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1664 | INFO_REALIGN_3_PRIME | chr21 | 36418017 | ||||
chr21:36418037
|
C | T | 1 | a0005c0006t0013 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1671C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1671 | chr21 | 36418037 | |||||
chr21:36418174
|
C | T | 6 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(3): Show | 22 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1808 | chr21 | 36418174 | |||||
chr21:36418267
|
C | T | 1 | a0001c0001t0032 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1901C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1901 | chr21 | 36418267 | |||||
chr21:36418290
|
G | A | 2 | a0001c0001t0004a0001c0001t0036 | 12 | NA18951.hp1 NA18957.hp2 NA18963.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1924G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1924 | chr21 | 36418290 | |||||
chr21:36418291
|
C | T | 1 | a0001c0001t0041 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1925 | chr21 | 36418291 | |||||
chr21:36418450
|
G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2084G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2084 | chr21 | 36418450 | |||||
chr21:36418451
|
T | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2085T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2085 | chr21 | 36418451 | |||||
chr21:36418453
|
A | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2087A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2087 | chr21 | 36418453 | |||||
chr21:36418454
|
G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2088G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2088 | chr21 | 36418454 | |||||
chr21:36418459
|
G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2093 | chr21 | 36418459 | |||||
chr21:36418460
|
G | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2094G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2094 | chr21 | 36418460 | |||||
chr21:36418464
|
G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2098G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2098 | chr21 | 36418464 | |||||
chr21:36418468
|
T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2102 | chr21 | 36418468 | |||||
chr21:36418469
|
T | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2103T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2103 | chr21 | 36418469 | |||||
chr21:36418471
|
T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2105T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2105 | chr21 | 36418471 | |||||
chr21:36418479
|
G | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2113 | chr21 | 36418479 | |||||
chr21:36418484
|
G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2118 | chr21 | 36418484 | |||||
chr21:36418496
|
A | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2130A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2130 | chr21 | 36418496 | |||||
chr21:36418499
|
A | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2133A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2133 | chr21 | 36418499 | |||||
chr21:36418501
|
G | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2135G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2135 | chr21 | 36418501 | |||||
chr21:36418502
|
G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2136G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2136 | chr21 | 36418502 | |||||
chr21:36418507
|
C | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2141 | chr21 | 36418507 | |||||
chr21:36418509
|
T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2143 | chr21 | 36418509 | |||||
chr21:36418511
|
T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2145T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2145 | chr21 | 36418511 | |||||
chr21:36418514
|
T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2148T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2148 | chr21 | 36418514 | |||||
chr21:36418515
|
T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2149 | chr21 | 36418515 | |||||
chr21:36418520
|
A | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2154 | chr21 | 36418520 | |||||
chr21:36418521
|
G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2155G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2155 | chr21 | 36418521 | |||||
chr21:36418522
|
C | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2156C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2156 | chr21 | 36418522 | |||||
chr21:36418525
|
C | A | 1 | a0001c0001t0038 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2159 | chr21 | 36418525 | |||||
chr21:36418525
|
C | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2159 | chr21 | 36418525 | |||||
chr21:36418526
|
C | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2160C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2160 | chr21 | 36418526 | |||||
chr21:36418527
|
T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2161T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2161 | chr21 | 36418527 | |||||
chr21:36418531
|
T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2165 | chr21 | 36418531 | |||||
chr21:36418532
|
C | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2166 | chr21 | 36418532 | |||||
chr21:36418534
|
T | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2168T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2168 | chr21 | 36418534 | |||||
chr21:36418535
|
G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2169G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2169 | chr21 | 36418535 | |||||
chr21:36418536
|
G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2170G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2170 | chr21 | 36418536 | |||||
chr21:36418539
|
A | T | 1 | a0002c0002t0046 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2173 | chr21 | 36418539 | |||||
chr21:36418540
|
T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2174T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2174 | chr21 | 36418540 | |||||
chr21:36418544
|
T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2178T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2178 | chr21 | 36418544 | |||||
chr21:36418563
|
G | C | 2 | a0001c0001t0014a0001c0001t0023 | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2197G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2197 | chr21 | 36418563 | |||||
chr21:36418831
|
A | C | 1 | a0001c0001t0040 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2465A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2465 | chr21 | 36418831 | |||||
chr21:36418848
|
C | CA | 20 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(17): Show | 67 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2497dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2498 | INFO_REALIGN_3_PRIME | chr21 | 36418848 | ||||
chr21:36418848
|
C | CAA | 4 | a0001c0001t0010a0002c0002t0010a0002c0002t0012others(1): Show | 9 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2496_*2497dupAA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2498 | INFO_REALIGN_3_PRIME | chr21 | 36418848 | ||||
chr21:36418848
|
CA | C | 4 | a0001c0001t0015a0001c0001t0018a0001c0001t0025others(1): Show | 7 | HG00323.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2497delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2497 | INFO_REALIGN_3_PRIME | chr21 | 36418848 | ||||
chr21:36419012
|
G | A | 1 | a0001c0001t0039 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2646G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2646 | chr21 | 36419012 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:36385505
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-78+54G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385505 | ||||||
chr21:36385512
|
A | T | 1 | a0001c0001t0022g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-78+61A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385512 | ||||||
chr21:36385523
|
G | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0003g0013others(27): Show | 30 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.-78+72G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385523 | ||||||
chr21:36385643
|
C | T | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-78+192C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385643 | ||||||
chr21:36385859
|
CTGGATGT others(20): Show |
C | 1 | a0001c0001t0035g0327 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-77-193_-77-167del others(27): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 36385859 | |||||
chr21:36385873
|
G | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77-187G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385873 | ||||||
chr21:36386270
|
G | A | 1 | a0001c0001t0008g0043 | 1 | HG02293.hp1 | splice_region_variant&intron_variant | LOW | c.126+8G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386270 | ||||||
chr21:36386677
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126+415G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386677 | ||||||
chr21:36386717
|
C | CT | 9 | a0001c0001t0001g0041a0001c0001t0004g0326a0001c0001t0009g0034others(6): Show | 9 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+469dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36386717 | |||||
chr21:36386759
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.126+497G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386759 | ||||||
chr21:36386801
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+539T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386801 | ||||||
chr21:36387010
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0034g0054 | 2 | HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.127-588G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387010 | ||||||
chr21:36387213
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-385A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387213 | ||||||
chr21:36387219
|
G | GT | 30 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(27): Show | 31 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-375dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387219 | |||||
chr21:36387219
|
G | GTTTTTT | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-375_127-374ins others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387219 | |||||
chr21:36387219
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-375_127-374ins others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387219 | |||||
chr21:36387223
|
TG | T | 3 | a0005c0006t0013g0292a0005c0006t0013g0293a0005c0006t0013g0294 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.127-374delG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387223 | ||||||
chr21:36387224
|
G | GT | 12 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0214others(9): Show | 12 | HG01243.hp1 HG01516.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-358dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387224 | |||||
chr21:36387224
|
G | GTT | 81 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(78): Show | 87 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.127-359_127-358dup others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387224 | |||||
chr21:36387224
|
G | T | 42 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(39): Show | 43 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-374G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387224 | ||||||
chr21:36387393
|
T | A | 3 | a0003c0003t0001g0055a0003c0003t0001g0056a0003c0003t0001g0207 | 3 | HG00642.hp1 HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.127-205T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387393 | ||||||
chr21:36387581
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-17T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387581 | ||||||
chr21:36387757
|
C | G | 1 | a0001c0001t0002g0291 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.259+27C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36387757 | ||||||
chr21:36387820
|
C | CT | 24 | a0001c0001t0001g0041a0001c0001t0002g0204a0001c0001t0002g0205others(21): Show | 24 | HG00741.hp1 HG01109.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.259+105dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36387820 | |||||
chr21:36387820
|
CTT | C | 6 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+104_259+105del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36387820 | |||||
chr21:36387848
|
C | T | 3 | a0005c0006t0013g0292a0005c0006t0013g0293a0005c0006t0013g0294 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.259+118C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36387848 | ||||||
chr21:36387975
|
C | T | 20 | a0001c0001t0001g0016a0001c0001t0003g0018a0001c0001t0003g0019others(17): Show | 20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.259+245C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36387975 | ||||||
chr21:36388103
|
G | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259+373G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388103 | ||||||
chr21:36388250
|
C | G | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+520C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388250 | ||||||
chr21:36388448
|
G | T | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+718G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388448 | ||||||
chr21:36388450
|
A | C | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259+720A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388450 | ||||||
chr21:36388468
|
G | GT | 19 | a0001c0001t0001g0041a0001c0001t0001g0192a0001c0001t0001g0193others(16): Show | 19 | HG00323.hp2 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.259+758dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388468 | |||||
chr21:36388468
|
GT | G | 16 | a0001c0001t0001g0061a0001c0001t0002g0216a0001c0001t0002g0217others(13): Show | 16 | HG00323.hp1 HG00741.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.259+758delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388468 | |||||
chr21:36388468
|
GTT | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(35): Show | 39 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.259+757_259+758del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388468 | |||||
chr21:36388469
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.259+739T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388469 | ||||||
chr21:36388496
|
TCTCACTG others(83): Show |
T | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | NA18981.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.259+772_259+861del others(90): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388496 | |||||
chr21:36388546
|
A | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(31): Show | 35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.259+816A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388546 | ||||||
chr21:36388611
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+881C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388611 | ||||||
chr21:36388694
|
T | C | 90 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(87): Show | 96 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.259+964T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388694 | ||||||
chr21:36388759
|
G | A | 3 | a0001c0001t0002g0204a0001c0001t0002g0221a0001c0001t0002g0222 | 3 | HG02132.hp1 NA18951.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.259+1029G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388759 | ||||||
chr21:36388762
|
C | T | 19 | a0001c0001t0001g0016a0001c0001t0003g0018a0001c0001t0003g0019others(16): Show | 19 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.259+1032C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388762 | ||||||
chr21:36388800
|
A | G | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1070A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388800 | ||||||
chr21:36388901
|
C | T | 1 | a0001c0001t0039g0189 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.259+1171C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388901 | ||||||
chr21:36389037
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.259+1307C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389037 | ||||||
chr21:36389066
|
G | A | 199 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0016others(196): Show | 208 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.259+1336G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389066 | ||||||
chr21:36389068
|
CGGTACCC others(22): Show |
C | 1 | a0001c0001t0007g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.259+1340_259+1368d others(31): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389068 | |||||
chr21:36389191
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.259+1461A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389191 | ||||||
chr21:36389203
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1473G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389203 | ||||||
chr21:36389220
|
A | T | 1 | a0001c0001t0004g0283 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.259+1490A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389220 | ||||||
chr21:36389408
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1678T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389408 | ||||||
chr21:36389474
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1744T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389474 | ||||||
chr21:36389513
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1783G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389513 | ||||||
chr21:36389571
|
C | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+1841C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389571 | ||||||
chr21:36389604
|
C | CA | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG00597.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+1891dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389604 | |||||
chr21:36389604
|
C | CAA | 9 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(6): Show | 9 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.259+1890_259+1891d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389604 | |||||
chr21:36389604
|
CA | C | 6 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0007g0085others(3): Show | 6 | HG01943.hp2 HG02486.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+1891delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389604 | |||||
chr21:36389681
|
TCTAAAGT others(10): Show |
T | 90 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(87): Show | 96 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.260-1869_260-1853d others(19): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389681 | ||||||
chr21:36389758
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0026g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.260-1793_260-1792i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389758 | ||||||
chr21:36389758
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0025g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.260-1793_260-1792i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389758 | ||||||
chr21:36389759
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0005g0297 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.260-1791_260-1790i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
A | ATG | 17 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0167others(14): Show | 18 | HG00408.hp2 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-1751_260-1750d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
A | ATGTG | 16 | a0001c0001t0001g0057a0001c0001t0001g0174a0001c0001t0001g0175others(13): Show | 16 | HG00408.hp1 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.260-1753_260-1750d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
A | ATGTGTG | 3 | a0001c0001t0001g0183a0001c0001t0001g0199a0002c0002t0010g0078 | 3 | HG01175.hp1 NA18956.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.260-1755_260-1750d others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0184a0001c0001t0008g0047a0001c0001t0008g0048 | 3 | HG00642.hp2 HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.260-1757_260-1750d others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
A | G | 2 | a0001c0001t0025g0052a0001c0001t0026g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.260-1792A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389759 | ||||||
chr21:36389759
|
ATG | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 17 | HG00673.hp1 HG00738.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-1751_260-1750d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
ATGTG | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0091others(27): Show | 31 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.260-1753_260-1750d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
ATGTGTG | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0090others(5): Show | 8 | HG01123.hp1 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1755_260-1750d others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389759
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.260-1759_260-1750d others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | |||||
chr21:36389761
|
G | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(29): Show | 33 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.260-1790G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389761 | ||||||
chr21:36389796
|
T | C | 1 | a0001c0001t0009g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.260-1755T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389796 | ||||||
chr21:36389796
|
T | TGC | 3 | a0001c0001t0001g0041a0001c0001t0009g0040a0001c0001t0027g0036 | 3 | HG02280.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.260-1754_260-1753i others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389796 | |||||
chr21:36389798
|
T | C | 15 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0002g0221others(12): Show | 15 | HG01952.hp2 HG02109.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-1753T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389798 | ||||||
chr21:36389798
|
T | TGC | 4 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0002g0229others(1): Show | 4 | HG00741.hp1 NA18612.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1752_260-1751i others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | |||||
chr21:36389798
|
T | TGCGC | 4 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0231others(1): Show | 4 | HG03490.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1752_260-1751i others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | |||||
chr21:36389798
|
T | TGCGCGCG others(11): Show |
2 | a0001c0001t0001g0011a0001c0001t0007g0298 | 3 | HG03098.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.260-1752_260-1751i others(20): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | |||||
chr21:36389798
|
T | TGCGCGCG others(13): Show |
1 | a0001c0001t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-1752_260-1751i others(22): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | |||||
chr21:36389800
|
T | C | 33 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0069others(30): Show | 34 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.260-1751T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389800 | ||||||
chr21:36389800
|
T | TGC | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 9 | HG00323.hp2 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-1744_260-1743d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGCGC | 28 | a0001c0001t0001g0016a0001c0001t0001g0285a0001c0001t0002g0219others(25): Show | 28 | HG01975.hp2 HG01981.hp1 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.260-1746_260-1743d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGCGCGCG others(1): Show |
3 | a0001c0001t0003g0025a0001c0001t0005g0297a0001c0001t0011g0017 | 3 | HG01978.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1743d others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGCGTGCG others(3): Show |
2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.260-1748_260-1747i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGC | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0003t0001g0191 | 3 | HG01099.hp2 HG01433.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGCGC | 34 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0002g0002others(31): Show | 39 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGCGCG others(1): Show |
7 | a0001c0001t0002g0272a0001c0001t0003g0026a0001c0001t0003g0027others(4): Show | 7 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGCGCG others(15): Show |
1 | a0001c0001t0006g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(1): Show |
14 | a0001c0001t0001g0053a0001c0001t0001g0284a0001c0001t0002g0010others(11): Show | 15 | HG00558.hp1 HG00558.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(3): Show |
5 | a0001c0001t0002g0289a0001c0001t0003g0013a0001c0001t0003g0022others(2): Show | 5 | HG01167.hp2 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(5): Show |
2 | a0004c0004t0003g0029a0005c0006t0013g0292 | 2 | HG01169.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(11): Show |
1 | a0001c0001t0006g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(20): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(13): Show |
1 | a0001c0001t0006g0301 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(22): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(15): Show |
1 | a0001c0001t0017g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGCG others(19): Show |
1 | a0001c0001t0001g0303 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(28): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(3): Show |
5 | a0001c0001t0001g0077a0001c0001t0002g0280a0001c0001t0002g0281others(2): Show | 5 | HG01255.hp2 HG02622.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(5): Show |
3 | a0001c0001t0003g0023a0004c0004t0003g0030a0004c0004t0003g0033 | 3 | HG00280.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0005g0304a0005c0006t0013g0293 | 2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(16): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0024g0305 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(18): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0005g0323 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(22): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0017g0306 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0006g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(5): Show |
7 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0015g0080others(4): Show | 7 | HG01106.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0003g0014a0001c0001t0009g0039 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(16): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(9): Show |
4 | a0001c0001t0005g0312a0001c0001t0005g0313a0001c0001t0005g0314others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(18): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0006g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(25): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0028g0296 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(24): Show |
1 | a0001c0001t0001g0316 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(33): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(7): Show |
3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0034g0054 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(16): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0005g0317a0005c0006t0013g0294 | 2 | HG00639.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(20): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0084 | 3 | HG01257.hp1 HG01258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(18): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(25): Show |
1 | a0001c0001t0001g0318 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(34): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(15): Show |
2 | a0001c0001t0005g0319a0001c0001t0005g0324 | 2 | HG00733.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(36): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389800
|
T | TGTGTGTG others(32): Show |
1 | a0001c0001t0001g0320 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(41): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | |||||
chr21:36389802
|
C | T | 8 | a0001c0001t0007g0182a0001c0001t0022g0328a0001c0001t0025g0052others(5): Show | 8 | HG01109.hp1 HG01175.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1749C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389802 | ||||||
chr21:36389830
|
A | G | 170 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0041others(167): Show | 177 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.260-1721A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389830 | ||||||
chr21:36389835
|
G | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.260-1716G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389835 | ||||||
chr21:36389988
|
G | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0016others(193): Show | 204 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.260-1563G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389988 | ||||||
chr21:36390028
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0192 | 2 | NA18997.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.260-1523C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390028 | ||||||
chr21:36390039
|
G | A | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1512G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390039 | ||||||
chr21:36390073
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 9 | HG00597.hp2 HG01192.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-1478C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390073 | ||||||
chr21:36390147
|
A | G | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1404A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390147 | ||||||
chr21:36390287
|
T | C | 31 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(28): Show | 32 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.260-1264T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390287 | ||||||
chr21:36390304
|
G | A | 34 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(31): Show | 35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.260-1247G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390304 | ||||||
chr21:36390333
|
C | CA | 40 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0041others(37): Show | 41 | HG00280.hp2 HG00408.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.260-1200dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | |||||
chr21:36390333
|
C | CAAAAG | 7 | a0001c0001t0002g0205a0001c0001t0002g0247a0001c0001t0002g0248others(4): Show | 7 | HG01981.hp1 NA18940.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-1214_260-1213i others(7): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | |||||
chr21:36390333
|
C | CAAAAGA | 79 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0285others(76): Show | 85 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.260-1214_260-1213i others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | |||||
chr21:36390333
|
CA | C | 11 | a0001c0001t0001g0091a0001c0001t0001g0156a0001c0001t0001g0199others(8): Show | 11 | HG02293.hp1 HG02630.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-1200delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | |||||
chr21:36390339
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.260-1212A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390339 | ||||||
chr21:36390348
|
A | G | 1 | a0001c0001t0040g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260-1203A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390348 | ||||||
chr21:36390400
|
A | G | 4 | a0001c0001t0016g0202a0001c0001t0016g0206a0001c0001t0016g0215others(1): Show | 4 | HG00741.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1151A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390400 | ||||||
chr21:36390503
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.260-1048A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390503 | ||||||
chr21:36390524
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.260-1027A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390524 | ||||||
chr21:36390666
|
T | C | 44 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(41): Show | 45 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.260-885T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390666 | ||||||
chr21:36390885
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.260-666G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390885 | ||||||
chr21:36391054
|
A | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 310 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.260-497A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391054 | ||||||
chr21:36391076
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-475T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391076 | ||||||
chr21:36391109
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-442A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391109 | ||||||
chr21:36391150
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.260-401G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391150 | ||||||
chr21:36391262
|
T | C | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.260-289T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391262 | ||||||
chr21:36391369
|
C | T | 11 | a0001c0001t0006g0295a0001c0001t0006g0300a0001c0001t0006g0301others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-182C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391369 | ||||||
chr21:36391442
|
C | T | 2 | a0001c0001t0005g0314a0001c0001t0005g0315 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.260-109C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391442 | ||||||
chr21:36391459
|
G | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-92G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391459 | ||||||
chr21:36391463
|
C | CA | 7 | a0001c0001t0001g0058a0001c0001t0001g0303a0001c0001t0002g0251others(4): Show | 7 | HG02148.hp1 HG03098.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-71dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36391463 | |||||
chr21:36391463
|
CA | C | 24 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0091others(21): Show | 24 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.260-71delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36391463 | |||||
chr21:36391481
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0016others(55): Show | 60 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.260-70T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391481 | ||||||
chr21:36391495
|
C | A | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-56C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391495 | ||||||
chr21:36391685
|
C | T | 1 | a0001c0001t0022g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.377+17C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391685 | ||||||
chr21:36391687
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.377+19T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391687 | ||||||
chr21:36391778
|
G | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.377+110G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391778 | ||||||
chr21:36391831
|
C | T | 1 | a0001c0001t0028g0296 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.377+163C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391831 | ||||||
chr21:36391907
|
A | AT | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 129 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.377+269dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | |||||
chr21:36391907
|
A | ATT | 30 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0106others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.377+268_377+269dup others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | |||||
chr21:36391907
|
A | ATTT | 19 | a0001c0001t0001g0153a0001c0001t0001g0320a0001c0001t0003g0014others(16): Show | 19 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.377+267_377+269dup others(3): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | |||||
chr21:36391907
|
A | ATTTT | 19 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(16): Show | 20 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.377+266_377+269dup others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | |||||
chr21:36391907
|
A | ATTTTT | 6 | a0001c0001t0001g0318a0001c0001t0006g0300a0001c0001t0017g0302others(3): Show | 6 | HG01358.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.377+265_377+269dup others(5): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | |||||
chr21:36391907
|
AT | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0222others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.377+269delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | |||||
chr21:36392078
|
C | T | 2 | a0001c0001t0025g0052a0001c0001t0026g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.377+410C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392078 | ||||||
chr21:36392088
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.377+420G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392088 | ||||||
chr21:36392152
|
A | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.377+484A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392152 | ||||||
chr21:36392265
|
C | T | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+597C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392265 | ||||||
chr21:36392308
|
C | G | 86 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(83): Show | 92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.377+640C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392308 | ||||||
chr21:36392390
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.377+722C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392390 | ||||||
chr21:36392402
|
C | G | 7 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(4): Show | 7 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.377+734C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392402 | ||||||
chr21:36392452
|
C | CG | 19 | a0001c0001t0001g0077a0001c0001t0001g0113a0001c0001t0001g0116others(16): Show | 19 | HG02109.hp2 HG02738.hp2 HG02886.hp2 others(16): Show |
intron_variant | MODIFIER | c.377+788dupG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36392452 | |||||
chr21:36392460
|
C | T | 11 | a0001c0001t0002g0246a0001c0001t0003g0049a0001c0001t0008g0043others(8): Show | 11 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.377+792C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392460 | ||||||
chr21:36392476
|
C | A | 1 | a0001c0001t0001g0252 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.377+808C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392476 | ||||||
chr21:36392512
|
G | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.377+844G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392512 | ||||||
chr21:36392512
|
G | GC | 14 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0172others(11): Show | 14 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.377+850dupC | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36392512 | |||||
chr21:36392513
|
C | T | 1 | a0001c0001t0028g0296 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.377+845C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392513 | ||||||
chr21:36392526
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+858G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392526 | ||||||
chr21:36392529
|
C | T | 1 | a0001c0001t0038g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.377+861C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392529 | ||||||
chr21:36392542
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.377+874C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392542 | ||||||
chr21:36392546
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.377+878C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392546 | ||||||
chr21:36392547
|
G | A | 1 | a0001c0001t0023g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377+879G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392547 | ||||||
chr21:36392583
|
C | T | 1 | a0001c0001t0040g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377+915C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392583 | ||||||
chr21:36392593
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+925T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392593 | ||||||
chr21:36392626
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.377+958G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392626 | ||||||
chr21:36392652
|
G | A | 21 | a0001c0001t0001g0016a0001c0001t0003g0013a0001c0001t0003g0014others(18): Show | 21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.377+984G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392652 | ||||||
chr21:36392667
|
C | T | 1 | a0001c0001t0007g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.377+999C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392667 | ||||||
chr21:36392733
|
C | T | 21 | a0001c0001t0001g0016a0001c0001t0003g0013a0001c0001t0003g0014others(18): Show | 21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.377+1065C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392733 | ||||||
chr21:36392776
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.377+1108C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392776 | ||||||
chr21:36392804
|
C | CG | 5 | a0001c0001t0001g0172a0001c0001t0002g0253a0001c0001t0002g0280others(2): Show | 5 | HG01433.hp2 HG03516.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.377+1140dupG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36392804 | |||||
chr21:36392861
|
G | A | 5 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0268others(2): Show | 5 | HG02257.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.377+1193G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392861 | ||||||
chr21:36392967
|
C | G | 30 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0003g0013others(27): Show | 30 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.377+1299C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392967 | ||||||
chr21:36392995
|
C | T | 1 | a0001c0001t0034g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.377+1327C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392995 | ||||||
chr21:36393013
|
C | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0170 | 2 | HG00741.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.377+1345C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393013 | ||||||
chr21:36393054
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.377+1386A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393054 | ||||||
chr21:36393058
|
G | A | 1 | a0001c0001t0009g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.377+1390G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393058 | ||||||
chr21:36393078
|
G | A | 1 | a0001c0001t0019g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.377+1410G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393078 | ||||||
chr21:36393228
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.378-1319C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393228 | ||||||
chr21:36393263
|
A | AT | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1281dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393263 | |||||
chr21:36393267
|
C | T | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1280C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393267 | ||||||
chr21:36393280
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1267G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393280 | ||||||
chr21:36393408
|
C | T | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.378-1139C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393408 | ||||||
chr21:36393446
|
C | CT | 20 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0057others(17): Show | 20 | HG00408.hp1 HG01099.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.378-1078dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393446 | |||||
chr21:36393446
|
CT | C | 24 | a0001c0001t0001g0117a0001c0001t0001g0175a0001c0001t0001g0177others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.378-1078delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393446 | |||||
chr21:36393446
|
CTT | C | 7 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(4): Show | 7 | HG01361.hp2 HG01943.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1079_378-1078d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393446 | |||||
chr21:36393472
|
A | G | 4 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(1): Show | 4 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-1075A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393472 | ||||||
chr21:36393477
|
G | A | 1 | a0001c0001t0033g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.378-1070G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393477 | ||||||
chr21:36393534
|
C | G | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-1013C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393534 | ||||||
chr21:36393646
|
G | GTACTGTT others(26): Show |
1 | a0001c0001t0007g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378-900_378-899ins others(33): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393646 | |||||
chr21:36393646
|
G | T | 3 | a0001c0001t0006g0300a0001c0001t0006g0301a0001c0001t0006g0311 | 3 | HG02055.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.378-901G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393646 | ||||||
chr21:36393653
|
C | T | 1 | a0001c0001t0007g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378-894C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393653 | ||||||
chr21:36393659
|
G | T | 1 | a0001c0001t0007g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378-888G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393659 | ||||||
chr21:36393733
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.378-814C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393733 | ||||||
chr21:36393803
|
T | C | 1 | a0001c0001t0009g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378-744T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393803 | ||||||
chr21:36393837
|
T | G | 170 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0041others(167): Show | 177 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.378-710T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393837 | ||||||
chr21:36393853
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-694T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393853 | ||||||
chr21:36393912
|
T | A | 34 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(31): Show | 35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.378-635T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393912 | ||||||
chr21:36393968
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-579T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393968 | ||||||
chr21:36393990
|
G | C | 170 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0041others(167): Show | 177 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.378-557G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393990 | ||||||
chr21:36394100
|
T | C | 44 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(41): Show | 45 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.378-447T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394100 | ||||||
chr21:36394137
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378-410C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394137 | ||||||
chr21:36394139
|
C | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-408C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394139 | ||||||
chr21:36394207
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(58): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.378-340G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394207 | ||||||
chr21:36394233
|
C | T | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.378-314C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394233 | ||||||
chr21:36394297
|
G | C | 3 | a0001c0001t0016g0202a0001c0001t0016g0206a0001c0001t0016g0215 | 3 | HG00741.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.378-250G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394297 | ||||||
chr21:36394336
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.378-211A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394336 | ||||||
chr21:36394429
|
T | TG | 90 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(87): Show | 96 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.378-117dupG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36394429 | |||||
chr21:36394468
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.378-79C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394468 | ||||||
chr21:36394479
|
G | A | 7 | a0002c0002t0010g0068a0002c0002t0010g0071a0002c0002t0010g0074others(4): Show | 8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-68G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394479 | ||||||
chr21:36394730
|
C | CT | 15 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0120others(12): Show | 15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+99dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36394730 | |||||
chr21:36394730
|
CT | C | 12 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(9): Show | 12 | HG00280.hp2 HG01169.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.481+99delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36394730 | |||||
chr21:36394749
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.481+99T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394749 | ||||||
chr21:36394913
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.481+263G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394913 | ||||||
chr21:36394920
|
C | T | 2 | a0001c0001t0001g0149a0003c0003t0001g0190 | 2 | HG00323.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.481+270C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394920 | ||||||
chr21:36394973
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+323T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394973 | ||||||
chr21:36394977
|
C | T | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+327C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394977 | ||||||
chr21:36395083
|
C | T | 1 | a0001c0001t0020g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.481+433C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395083 | ||||||
chr21:36395143
|
C | T | 12 | a0001c0001t0001g0041a0001c0001t0009g0034a0001c0001t0009g0035others(9): Show | 12 | HG01952.hp2 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.481+493C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395143 | ||||||
chr21:36395144
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.481+494G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395144 | ||||||
chr21:36395154
|
G | A | 1 | a0001c0001t0040g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481+504G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395154 | ||||||
chr21:36395171
|
A | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.481+521A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395171 | ||||||
chr21:36395294
|
C | G | 3 | a0001c0001t0002g0250a0001c0001t0002g0272a0001c0001t0002g0282 | 3 | NA18941.hp2 NA18992.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.481+644C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395294 | ||||||
chr21:36395764
|
A | AG | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+1114_481+1115i others(3): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395764 | ||||||
chr21:36395887
|
A | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0016others(193): Show | 204 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.481+1237A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395887 | ||||||
chr21:36396003
|
G | GT | 31 | a0001c0001t0001g0016a0001c0001t0002g0012a0001c0001t0003g0013others(28): Show | 31 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.481+1364dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396003 | |||||
chr21:36396014
|
T | C | 1 | a0001c0001t0045g0208 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481+1364T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396014 | ||||||
chr21:36396112
|
G | A | 7 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(4): Show | 7 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-1303G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396112 | ||||||
chr21:36396182
|
A | T | 170 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0041others(167): Show | 177 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.482-1233A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396182 | ||||||
chr21:36396202
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-1213G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396202 | ||||||
chr21:36396237
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0180a0001c0001t0001g0199others(1): Show | 4 | HG00408.hp1 NA18940.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1178C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396237 | ||||||
chr21:36396330
|
G | A | 13 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0172others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.482-1085G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396330 | ||||||
chr21:36396358
|
C | CA | 63 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0105others(60): Show | 69 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.482-1032dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396358
|
C | CAAA | 6 | a0001c0001t0005g0313a0001c0001t0005g0315a0001c0001t0008g0044others(3): Show | 6 | HG00639.hp2 HG01517.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-1034_482-1032d others(5): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396358
|
C | CAAAA | 12 | a0001c0001t0001g0320a0001c0001t0005g0297a0001c0001t0005g0312others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.482-1035_482-1032d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396358
|
C | CAAAAA | 14 | a0001c0001t0001g0299a0001c0001t0001g0303a0001c0001t0001g0316others(11): Show | 14 | HG01884.hp1 HG02148.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-1036_482-1032d others(7): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396358
|
C | CAAAAAA | 8 | a0001c0001t0001g0011a0001c0001t0001g0318a0001c0001t0001g0325others(5): Show | 9 | HG01106.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-1037_482-1032d others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396358
|
CA | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0069others(30): Show | 34 | HG00323.hp2 HG00423.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.482-1032delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396358
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-1041_482-1032d others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | |||||
chr21:36396538
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0009g0035a0001c0001t0009g0040others(1): Show | 4 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-877C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396538 | ||||||
chr21:36396598
|
G | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-817G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396598 | ||||||
chr21:36396603
|
C | T | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-812C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396603 | ||||||
chr21:36396653
|
C | CA | 34 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(31): Show | 35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.482-752dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396653 | |||||
chr21:36396653
|
CA | C | 10 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-752delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396653 | |||||
chr21:36396663
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-752A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396663 | ||||||
chr21:36396664
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-751G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396664 | ||||||
chr21:36396664
|
G | GA | 9 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-740dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396664 | |||||
chr21:36396684
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.482-731C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396684 | ||||||
chr21:36396825
|
C | G | 21 | a0001c0001t0001g0016a0001c0001t0003g0013a0001c0001t0003g0014others(18): Show | 21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.482-590C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396825 | ||||||
chr21:36396833
|
T | C | 170 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0041others(167): Show | 177 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.482-582T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396833 | ||||||
chr21:36396989
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0043g0212 | 2 | NA18988.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.482-426A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396989 | ||||||
chr21:36396991
|
TTCTCAGC others(4): Show |
T | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482-419_482-409del others(11): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396991 | |||||
chr21:36397135
|
C | T | 1 | a0005c0006t0013g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.482-280C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397135 | ||||||
chr21:36397233
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.482-182C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397233 | ||||||
chr21:36397279
|
A | G | 94 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(91): Show | 100 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.482-136A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397279 | ||||||
chr21:36397292
|
CT | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG00738.hp2 HG01257.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-121delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36397292 | |||||
chr21:36397352
|
A | G | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-63A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397352 | ||||||
chr21:36397390
|
G | C | 1 | a0001c0001t0035g0327 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.482-25G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397390 | ||||||
chr21:36397391
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0303a0001c0001t0003g0014 | 3 | HG02486.hp2 HG03471.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.482-24C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397391 | ||||||
chr21:36397392
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.482-23G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397392 | ||||||
chr21:36397402
|
G | GT | 9 | a0001c0001t0001g0099a0001c0001t0003g0201a0001c0001t0008g0043others(6): Show | 9 | HG00408.hp2 HG01192.hp1 HG01361.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.482-5dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36397402 | |||||
chr21:36397402
|
G | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00738.hp1 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-13G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397402 | ||||||
chr21:36397403
|
T | TG | 11 | a0001c0001t0005g0297a0001c0001t0005g0304a0001c0001t0005g0312others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-12_482-11insG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397403 | ||||||
chr21:36397554
|
A | G | 30 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0003g0013others(27): Show | 30 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.578+43A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397554 | ||||||
chr21:36397605
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | NA18966.hp1 NA18983.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.578+94C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397605 | ||||||
chr21:36397719
|
C | A | 1 | a0001c0001t0002g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.578+208C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397719 | ||||||
chr21:36397719
|
C | CT | 45 | a0001c0001t0001g0011a0001c0001t0001g0087a0001c0001t0001g0130others(42): Show | 46 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.578+229dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36397719 | |||||
chr21:36397719
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.578+208C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397719 | ||||||
chr21:36397719
|
CT | C | 13 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0092others(10): Show | 13 | HG01070.hp1 HG01070.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.578+229delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36397719 | |||||
chr21:36397719
|
CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.578+219_578+229del others(11): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36397719 | |||||
chr21:36397836
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0009g0035a0001c0001t0009g0040others(1): Show | 4 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+325T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397836 | ||||||
chr21:36397929
|
C | T | 15 | a0001c0001t0001g0252a0001c0001t0002g0002a0001c0001t0002g0204others(12): Show | 19 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+418C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397929 | ||||||
chr21:36397936
|
C | G | 1 | a0001c0001t0002g0280 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.578+425C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397936 | ||||||
chr21:36397985
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.578+474A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397985 | ||||||
chr21:36398055
|
AT | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0069others(15): Show | 19 | HG01167.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.578+559delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36398055 | |||||
chr21:36398113
|
T | C | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.578+602T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398113 | ||||||
chr21:36398198
|
G | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG00408.hp2 HG01978.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+687G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398198 | ||||||
chr21:36398273
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.578+762C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398273 | ||||||
chr21:36398341
|
G | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.578+830G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398341 | ||||||
chr21:36398609
|
G | A | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-912G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398609 | ||||||
chr21:36398712
|
G | C | 170 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0041others(167): Show | 177 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.579-809G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398712 | ||||||
chr21:36398766
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.579-755G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398766 | ||||||
chr21:36398772
|
T | A | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-749T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398772 | ||||||
chr21:36399034
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0183 | 2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.579-487C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399034 | ||||||
chr21:36399036
|
A | AT | 36 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0135others(33): Show | 36 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.579-467dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36399036 | |||||
chr21:36399036
|
AT | A | 10 | a0001c0001t0001g0214a0001c0001t0001g0320a0001c0001t0002g0204others(7): Show | 10 | HG00323.hp1 HG01167.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-467delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36399036 | |||||
chr21:36399036
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.579-476_579-467del others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36399036 | |||||
chr21:36399179
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.579-342C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399179 | ||||||
chr21:36399185
|
C | T | 4 | a0001c0001t0009g0034a0001c0001t0009g0037a0001c0001t0009g0038others(1): Show | 4 | HG03139.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-336C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399185 | ||||||
chr21:36399216
|
G | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-305G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399216 | ||||||
chr21:36399282
|
C | A | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-239C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399282 | ||||||
chr21:36399288
|
T | C | 100 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(97): Show | 106 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.579-233T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399288 | ||||||
chr21:36399303
|
C | T | 1 | a0001c0001t0007g0194 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.579-218C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399303 | ||||||
chr21:36399328
|
G | A | 19 | a0001c0001t0001g0016a0001c0001t0003g0018a0001c0001t0003g0019others(16): Show | 19 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.579-193G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399328 | ||||||
chr21:36399397
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(19): Show | 23 | HG01106.hp1 HG01167.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.579-124T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399397 | ||||||
chr21:36399507
|
T | C | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.579-14T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399507 | ||||||
chr21:36399706
|
A | G | 10 | a0001c0001t0003g0049a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.663+101A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36399706 | ||||||
chr21:36399848
|
C | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663+243C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36399848 | ||||||
chr21:36399991
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.663+386C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36399991 | ||||||
chr21:36400128
|
G | A | 1 | a0002c0002t0012g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.663+523G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400128 | ||||||
chr21:36400262
|
C | G | 3 | a0004c0004t0003g0028a0004c0004t0003g0029a0004c0004t0003g0033 | 3 | HG01167.hp2 HG01169.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.663+657C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400262 | ||||||
chr21:36400292
|
C | G | 85 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(82): Show | 91 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.663+687C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400292 | ||||||
chr21:36400348
|
G | A | 19 | a0001c0001t0001g0016a0001c0001t0003g0018a0001c0001t0003g0019others(16): Show | 19 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.663+743G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400348 | ||||||
chr21:36400394
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.663+789C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400394 | ||||||
chr21:36400421
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.663+816A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400421 | ||||||
chr21:36400457
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(17): Show | 21 | HG01106.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.663+852G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400457 | ||||||
chr21:36400540
|
C | T | 85 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(82): Show | 91 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.663+935C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400540 | ||||||
chr21:36400630
|
C | T | 1 | a0001c0001t0003g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.663+1025C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400630 | ||||||
chr21:36400658
|
C | T | 34 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(31): Show | 35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.663+1053C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400658 | ||||||
chr21:36400668
|
G | C | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.663+1063G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400668 | ||||||
chr21:36400690
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.663+1085A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400690 | ||||||
chr21:36400700
|
G | T | 7 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0027others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+1095G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400700 | ||||||
chr21:36400824
|
C | A | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.663+1219C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400824 | ||||||
chr21:36400833
|
C | T | 1 | a0001c0001t0045g0208 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.663+1228C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400833 | ||||||
chr21:36400866
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.663+1261G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400866 | ||||||
chr21:36400958
|
A | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(31): Show | 35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.663+1353A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400958 | ||||||
chr21:36400990
|
G | A | 2 | a0001c0001t0025g0052a0001c0001t0026g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.663+1385G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400990 | ||||||
chr21:36400996
|
G | A | 1 | a0001c0001t0009g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.663+1391G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400996 | ||||||
chr21:36401322
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.664-1436T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401322 | ||||||
chr21:36401349
|
T | C | 1 | a0005c0006t0013g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.664-1409T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401349 | ||||||
chr21:36401352
|
A | AATATATA others(17): Show |
1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.664-1400_664-1399i others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | |||||
chr21:36401352
|
A | AATATATT others(17): Show |
11 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-1180_664-1157d others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | |||||
chr21:36401352
|
A | AATATATT others(41): Show |
1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.664-1204_664-1157d others(50): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | |||||
chr21:36401352
|
AATATATT others(17): Show |
A | 8 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG00673.hp1 HG01981.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-1180_664-1157d others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | |||||
chr21:36401352
|
AATATATT others(41): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.664-1204_664-1157d others(50): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | |||||
chr21:36401371
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0003g0013others(36): Show | 39 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.664-1387C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401371 | ||||||
chr21:36401400
|
T | TATATATT others(15): Show |
1 | a0001c0001t0002g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.664-1351_664-1330d others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401400 | |||||
chr21:36401422
|
AAT | A | 84 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(81): Show | 90 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.664-1329_664-1328d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401422 | |||||
chr21:36401521
|
A | G | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-1237A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401521 | ||||||
chr21:36401525
|
AT | A | 22 | a0001c0001t0001g0316a0001c0001t0005g0304a0001c0001t0005g0314others(19): Show | 22 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.664-1228delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401525 | |||||
chr21:36401549
|
AT | A | 48 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0299others(45): Show | 49 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.664-1204delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401549 | |||||
chr21:36401549
|
ATTTTTAT others(18): Show |
A | 14 | a0001c0001t0005g0304a0001c0001t0005g0314a0001c0001t0005g0315others(11): Show | 14 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.664-1204_664-1180d others(27): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401549 | |||||
chr21:36401550
|
T | TTTTTATA others(16): Show |
1 | a0001c0001t0023g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.664-1203_664-1181d others(25): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401550 | |||||
chr21:36401550
|
TTTTTATA others(40): Show |
T | 7 | a0001c0001t0009g0034a0001c0001t0009g0037a0001c0001t0009g0038others(4): Show | 7 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1171_664-1125d others(49): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401550 | |||||
chr21:36401573
|
AT | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0041others(125): Show | 136 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.664-1180delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401573 | |||||
chr21:36401574
|
T | TTTTATAT others(39): Show |
1 | a0002c0002t0010g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-1181_664-1180i others(48): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401574 | |||||
chr21:36401574
|
TTTTTATA others(16): Show |
T | 29 | a0001c0001t0001g0016a0001c0001t0001g0322a0001c0001t0003g0013others(26): Show | 29 | HG00280.hp2 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.664-1156_664-1134d others(25): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401574 | |||||
chr21:36401597
|
A | AT | 111 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0053others(108): Show | 118 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.664-1157dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401597 | |||||
chr21:36401597
|
A | ATTTTATA others(17): Show |
17 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0172others(14): Show | 18 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.664-1148_664-1125d others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401597 | |||||
chr21:36401597
|
A | ATTTTTAT others(41): Show |
5 | a0002c0002t0010g0068a0002c0002t0010g0074a0002c0002t0010g0078others(2): Show | 5 | HG01123.hp2 HG01175.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1157_664-1156i others(50): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401597 | |||||
chr21:36401634
|
T | C | 8 | a0001c0001t0006g0295a0001c0001t0008g0043a0001c0001t0008g0044others(5): Show | 8 | HG00639.hp2 HG01361.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-1124T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401634 | ||||||
chr21:36401806
|
T | C | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-952T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401806 | ||||||
chr21:36401984
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.664-774G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401984 | ||||||
chr21:36401996
|
C | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-762C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401996 | ||||||
chr21:36402085
|
G | T | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.664-673G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402085 | ||||||
chr21:36402090
|
A | G | 14 | a0001c0001t0001g0091a0001c0001t0001g0097a0001c0001t0001g0098others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.664-668A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402090 | ||||||
chr21:36402102
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.664-656T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402102 | ||||||
chr21:36402383
|
C | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-375C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402383 | ||||||
chr21:36402459
|
A | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-299A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402459 | ||||||
chr21:36402506
|
C | T | 21 | a0001c0001t0001g0016a0001c0001t0003g0013a0001c0001t0003g0014others(18): Show | 21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.664-252C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402506 | ||||||
chr21:36402619
|
A | G | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-139A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402619 | ||||||
chr21:36402628
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.664-130A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402628 | ||||||
chr21:36402629
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.664-129G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402629 | ||||||
chr21:36402686
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.664-72G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402686 | ||||||
chr21:36402725
|
A | C | 1 | a0001c0001t0003g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.664-33A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402725 | ||||||
chr21:36402978
|
T | C | 86 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0284others(83): Show | 92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.757+127T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36402978 | ||||||
chr21:36403126
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.757+275G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403126 | ||||||
chr21:36403289
|
C | G | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.757+438C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403289 | ||||||
chr21:36403359
|
C | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(318): Show | 338 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.757+508C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403359 | ||||||
chr21:36403436
|
GACAGAGT others(3838): Show |
G | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.757+595_758-1471de others(1): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403436 | |||||
chr21:36403455
|
T | TA | 35 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0089others(32): Show | 36 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.757+629dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | |||||
chr21:36403455
|
TA | T | 28 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0211others(25): Show | 28 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.757+629delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | |||||
chr21:36403455
|
TAA | T | 17 | a0001c0001t0003g0032a0001c0001t0007g0298a0001c0001t0009g0034others(14): Show | 17 | HG00741.hp1 HG02109.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.757+628_757+629del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | |||||
chr21:36403455
|
TAAA | T | 33 | a0001c0001t0001g0011a0001c0001t0001g0299a0001c0001t0001g0303others(30): Show | 34 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+627_757+629del others(3): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | |||||
chr21:36403455
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.757+617_757+629del others(13): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | |||||
chr21:36403549
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.757+698G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403549 | ||||||
chr21:36403551
|
G | A | 7 | a0001c0001t0001g0090a0001c0001t0003g0022a0001c0001t0003g0023others(4): Show | 7 | HG00280.hp2 HG01243.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+700G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403551 | ||||||
chr21:36403861
|
G | A | 1 | a0001c0001t0024g0305 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.757+1010G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403861 | ||||||
chr21:36403903
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0002g0274 | 2 | HG00558.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.757+1052T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403903 | ||||||
chr21:36403986
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.757+1135C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403986 | ||||||
chr21:36404096
|
C | CT | 41 | a0001c0001t0001g0016a0001c0001t0001g0142a0001c0001t0001g0157others(38): Show | 41 | HG00438.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.757+1265dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404096 | |||||
chr21:36404096
|
CT | C | 15 | a0001c0001t0001g0053a0001c0001t0001g0082a0001c0001t0002g0243others(12): Show | 15 | HG01361.hp2 HG01943.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.757+1265delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404096 | |||||
chr21:36404160
|
C | T | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0020g0123others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.757+1309C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404160 | ||||||
chr21:36404203
|
C | T | 3 | a0001c0001t0003g0024a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.757+1352C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404203 | ||||||
chr21:36404290
|
G | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.757+1439G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404290 | ||||||
chr21:36404399
|
C | CT | 21 | a0001c0001t0003g0049a0001c0001t0003g0102a0001c0001t0005g0297others(18): Show | 21 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.757+1561dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404399 | |||||
chr21:36404412
|
T | A | 2 | a0001c0001t0031g0254a0003c0003t0001g0056 | 2 | HG00438.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.757+1561T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404412 | ||||||
chr21:36404413
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0101 | 2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.757+1562A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404413 | ||||||
chr21:36404464
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.757+1613C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404464 | ||||||
chr21:36404503
|
C | T | 14 | a0001c0001t0001g0041a0001c0001t0001g0158a0001c0001t0001g0159others(11): Show | 14 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.757+1652C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404503 | ||||||
chr21:36404558
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.757+1707C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404558 | ||||||
chr21:36404559
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0034g0054 | 2 | HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.757+1708G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404559 | ||||||
chr21:36404732
|
C | CT | 6 | a0001c0001t0002g0236a0001c0001t0002g0249a0001c0001t0014g0066others(3): Show | 6 | HG00741.hp1 HG01952.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+1908dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | |||||
chr21:36404732
|
CT | C | 54 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0001g0126others(51): Show | 60 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.757+1908delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | |||||
chr21:36404732
|
CTT | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 209 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.757+1907_757+1908d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | |||||
chr21:36404732
|
CTTT | C | 35 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0061others(32): Show | 36 | HG00280.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.757+1906_757+1908d others(5): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | |||||
chr21:36404757
|
T | A | 3 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0269 | 3 | HG02080.hp1 NA18979.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.757+1906T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404757 | ||||||
chr21:36404759
|
T | A | 1 | a0001c0001t0003g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.757+1908T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404759 | ||||||
chr21:36404927
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0142others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.757+2076A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404927 | ||||||
chr21:36404941
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.757+2090G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404941 | ||||||
chr21:36404982
|
G | A | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.757+2131G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404982 | ||||||
chr21:36405042
|
CGCCCA | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.757+2196_757+2200d others(7): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36405042 | |||||
chr21:36405043
|
G | A | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.757+2192G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405043 | ||||||
chr21:36405113
|
A | G | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.757+2262A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405113 | ||||||
chr21:36405327
|
A | G | 12 | a0001c0001t0006g0295a0001c0001t0006g0300a0001c0001t0006g0301others(9): Show | 12 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.757+2476A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405327 | ||||||
chr21:36405525
|
G | T | 1 | a0003c0003t0001g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.757+2674G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405525 | ||||||
chr21:36405560
|
G | A | 1 | a0001c0001t0038g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.757+2709G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405560 | ||||||
chr21:36405766
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.757+2915A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405766 | ||||||
chr21:36405929
|
A | G | 10 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0009g0034others(7): Show | 10 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.758-2832A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405929 | ||||||
chr21:36405942
|
T | C | 1 | a0002c0002t0046g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.758-2819T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405942 | ||||||
chr21:36405957
|
T | TA | 27 | a0001c0001t0005g0297a0001c0001t0005g0304a0001c0001t0005g0312others(24): Show | 27 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.758-2794dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36405957 | |||||
chr21:36405984
|
G | C | 1 | a0001c0001t0001g0188 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.758-2777G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405984 | ||||||
chr21:36406112
|
T | C | 3 | a0005c0006t0013g0292a0005c0006t0013g0293a0005c0006t0013g0294 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.758-2649T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406112 | ||||||
chr21:36406388
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.758-2373T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406388 | ||||||
chr21:36406532
|
C | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.758-2229C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406532 | ||||||
chr21:36406628
|
G | A | 1 | a0001c0001t0003g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.758-2133G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406628 | ||||||
chr21:36407080
|
T | C | 23 | a0001c0001t0005g0297a0001c0001t0005g0304a0001c0001t0005g0312others(20): Show | 23 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.758-1681T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407080 | ||||||
chr21:36407192
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.758-1569C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407192 | ||||||
chr21:36407285
|
G | A | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.758-1476G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407285 | ||||||
chr21:36407288
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1473T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407288 | ||||||
chr21:36407289
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1472G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407289 | ||||||
chr21:36407296
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1465T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407296 | ||||||
chr21:36407297
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1464G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407297 | ||||||
chr21:36407300
|
T | TA | 8 | a0001c0001t0001g0146a0001c0001t0001g0199a0001c0001t0002g0219others(5): Show | 8 | HG02132.hp1 HG02293.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-1444dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36407300 | |||||
chr21:36407300
|
TA | T | 53 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0002g0218others(50): Show | 53 | HG00280.hp2 HG00733.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.758-1444delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36407300 | |||||
chr21:36407301
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1460A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407301 | ||||||
chr21:36407317
|
A | T | 3 | a0001c0001t0009g0035a0001c0001t0009g0040a0001c0001t0027g0036 | 3 | HG02717.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.758-1444A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407317 | ||||||
chr21:36407317
|
AG | A | 7 | a0002c0002t0010g0068a0002c0002t0010g0071a0002c0002t0010g0074others(4): Show | 8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-1443delG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407317 | ||||||
chr21:36407418
|
C | T | 1 | a0001c0001t0002g0276 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.758-1343C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407418 | ||||||
chr21:36407850
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.758-911T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407850 | ||||||
chr21:36408344
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.758-417A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408344 | ||||||
chr21:36408453
|
G | C | 1 | a0001c0001t0007g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.758-308G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408453 | ||||||
chr21:36408524
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.758-237C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408524 | ||||||
chr21:36408580
|
G | A | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.758-181G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408580 | ||||||
chr21:36408677
|
C | G | 2 | a0001c0001t0006g0301a0001c0001t0006g0311 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.758-84C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408677 | ||||||
chr21:36408748
|
C | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0010others(39): Show | 48 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.758-13C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408748 | ||||||
chr21:36408885
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827+55G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36408885 | ||||||
chr21:36408948
|
G | A | 2 | a0001c0001t0005g0297a0001c0001t0005g0317 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.827+118G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36408948 | ||||||
chr21:36409033
|
T | C | 1 | a0001c0001t0002g0236 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.827+203T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409033 | ||||||
chr21:36409046
|
G | C | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+216G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409046 | ||||||
chr21:36409109
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.828-265C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409109 | ||||||
chr21:36409158
|
A | AT | 42 | a0001c0001t0001g0141a0001c0001t0001g0183a0001c0001t0002g0205others(39): Show | 42 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.828-194dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr21 | 36409158 | |||||
chr21:36409158
|
A | ATT | 21 | a0001c0001t0003g0013a0001c0001t0003g0018a0001c0001t0003g0019others(18): Show | 21 | HG00280.hp2 HG01106.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.828-195_828-194dup others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr21 | 36409158 | |||||
chr21:36409213
|
C | A | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.828-161C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409213 | ||||||
chr21:36409694
|
C | T | 1 | a0001c0001t0009g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.919+229C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409694 | ||||||
chr21:36409788
|
G | A | 1 | a0003c0003t0001g0210 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.919+323G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409788 | ||||||
chr21:36409793
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG02074.hp1 HG02698.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+328C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409793 | ||||||
chr21:36409836
|
G | A | 4 | a0001c0001t0009g0034a0001c0001t0009g0037a0001c0001t0009g0038others(1): Show | 4 | HG03139.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+371G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409836 | ||||||
chr21:36409859
|
T | G | 2 | a0001c0001t0003g0049a0001c0001t0003g0102 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.919+394T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409859 | ||||||
chr21:36409867
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.919+402T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409867 | ||||||
chr21:36409884
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.919+419A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409884 | ||||||
chr21:36409921
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0112 | 3 | HG02148.hp1 HG03688.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.919+456G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409921 | ||||||
chr21:36409967
|
C | CT | 10 | a0001c0001t0003g0200a0001c0001t0008g0043a0001c0001t0008g0044others(7): Show | 10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+516dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36409967 | |||||
chr21:36409967
|
CT | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0173a0001c0001t0002g0276others(3): Show | 6 | HG00408.hp2 HG02698.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+516delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36409967 | |||||
chr21:36410002
|
C | T | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.919+537C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410002 | ||||||
chr21:36410045
|
A | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.919+580A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410045 | ||||||
chr21:36410182
|
C | T | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.919+717C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410182 | ||||||
chr21:36410198
|
G | T | 20 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(17): Show | 20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+733G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410198 | ||||||
chr21:36410628
|
A | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-835A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410628 | ||||||
chr21:36410674
|
C | CT | 20 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(17): Show | 20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-775dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36410674 | |||||
chr21:36410674
|
CT | C | 6 | a0001c0001t0002g0282a0002c0002t0010g0068a0002c0002t0010g0071others(3): Show | 6 | HG01109.hp1 HG01175.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-775delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36410674 | |||||
chr21:36410722
|
A | G | 1 | a0001c0001t0002g0227 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.920-741A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410722 | ||||||
chr21:36410729
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0090others(8): Show | 12 | HG01167.hp1 HG01884.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.920-734C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410729 | ||||||
chr21:36410747
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0001g0170 | 3 | HG00741.hp2 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.920-716G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410747 | ||||||
chr21:36410908
|
G | A | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.920-555G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410908 | ||||||
chr21:36411116
|
CT | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.920-332delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36411116 | |||||
chr21:36411116
|
CTT | C | 10 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0027others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-333_920-332del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36411116 | |||||
chr21:36411199
|
C | T | 1 | a0001c0001t0008g0047 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.920-264C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36411199 | ||||||
chr21:36411361
|
G | A | 3 | a0001c0001t0002g0257a0001c0001t0002g0275a0001c0001t0031g0254 | 3 | HG00438.hp1 HG00558.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.920-102G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36411361 | ||||||
chr21:36411400
|
C | G | 1 | a0001c0001t0002g0243 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.920-63C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36411400 | ||||||
chr21:36411614
|
T | G | 12 | a0001c0001t0006g0295a0001c0001t0006g0300a0001c0001t0006g0301others(9): Show | 12 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1061+10T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411614 | ||||||
chr21:36411739
|
A | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0154 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1061+135A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411739 | ||||||
chr21:36411761
|
C | T | 1 | a0001c0001t0011g0017 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1061+157C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411761 | ||||||
chr21:36411772
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1061+168G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411772 | ||||||
chr21:36411803
|
A | C | 7 | a0002c0002t0010g0068a0002c0002t0010g0071a0002c0002t0010g0074others(4): Show | 8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+199A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411803 | ||||||
chr21:36411877
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0199 | 2 | NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1061+273C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411877 | ||||||
chr21:36411966
|
G | T | 2 | a0001c0001t0001g0115a0001c0001t0035g0327 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1061+362G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411966 | ||||||
chr21:36412020
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1061+416G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412020 | ||||||
chr21:36412069
|
C | T | 1 | a0001c0007t0003g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1061+465C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412069 | ||||||
chr21:36412137
|
C | A | 1 | a0001c0001t0001g0077 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1061+533C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412137 | ||||||
chr21:36412256
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1062-628G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412256 | ||||||
chr21:36412342
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0069others(9): Show | 13 | HG01257.hp1 HG01258.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1062-542C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412342 | ||||||
chr21:36412369
|
G | GT | 6 | a0001c0001t0001g0107a0001c0001t0001g0171a0001c0001t0006g0311others(3): Show | 6 | HG01257.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062-505dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr21 | 36412369 | |||||
chr21:36412384
|
CAG | C | 2 | a0002c0002t0012g0003a0002c0002t0012g0075 | 3 | HG02145.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1062-497_1062-496d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr21 | 36412384 | |||||
chr21:36412422
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1062-462C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412422 | ||||||
chr21:36412426
|
C | T | 7 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(4): Show | 7 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1062-458C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412426 | ||||||
chr21:36412445
|
C | T | 5 | a0001c0001t0002g0257a0001c0001t0002g0275a0001c0001t0003g0200others(2): Show | 5 | HG00438.hp1 HG00558.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-439C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412445 | ||||||
chr21:36412494
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1062-390G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412494 | ||||||
chr21:36412504
|
C | T | 2 | a0002c0002t0012g0003a0002c0002t0012g0075 | 3 | HG02145.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1062-380C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412504 | ||||||
chr21:36412508
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1062-376C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412508 | ||||||
chr21:36413374
|
C | A | 1 | a0001c0001t0007g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1493+59C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413374 | ||||||
chr21:36413501
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1493+186A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413501 | ||||||
chr21:36413685
|
T | C | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+370T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413685 | ||||||
chr21:36413696
|
G | A | 2 | a0001c0001t0003g0049a0001c0001t0003g0102 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1493+381G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413696 | ||||||
chr21:36413706
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 238 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1493+391C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413706 | ||||||
chr21:36413978
|
G | A | 6 | a0001c0001t0002g0250a0001c0001t0002g0253a0001c0001t0002g0256others(3): Show | 6 | NA18941.hp2 NA18957.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1493+663G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413978 | ||||||
chr21:36414034
|
G | A | 7 | a0001c0001t0009g0034a0001c0001t0009g0035a0001c0001t0009g0037others(4): Show | 7 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1493+719G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414034 | ||||||
chr21:36414050
|
C | T | 4 | a0001c0001t0016g0202a0001c0001t0016g0206a0001c0001t0016g0215others(1): Show | 4 | HG00741.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+735C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414050 | ||||||
chr21:36414068
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0183 | 2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1493+753G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414068 | ||||||
chr21:36414175
|
C | T | 1 | a0001c0001t0024g0305 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1493+860C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414175 | ||||||
chr21:36414220
|
C | T | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+905C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414220 | ||||||
chr21:36414231
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0101 | 2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1493+916C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414231 | ||||||
chr21:36414312
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1494-983C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414312 | ||||||
chr21:36414379
|
G | T | 18 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0022others(15): Show | 18 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1494-916G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414379 | ||||||
chr21:36414451
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1494-844T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414451 | ||||||
chr21:36414470
|
C | T | 4 | a0001c0001t0014g0065a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494-825C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414470 | ||||||
chr21:36414642
|
T | A | 20 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(17): Show | 20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1494-653T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414642 | ||||||
chr21:36414654
|
C | A | 3 | a0001c0001t0003g0024a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1494-641C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414654 | ||||||
chr21:36414719
|
C | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494-576C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414719 | ||||||
chr21:36414765
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0015g0060 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1494-530C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414765 | ||||||
chr21:36414869
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0077others(7): Show | 11 | HG01257.hp1 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1494-426C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414869 | ||||||
chr21:36414899
|
C | T | 3 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0007t0003g0076 | 3 | HG02559.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1494-396C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414899 | ||||||
chr21:36414972
|
C | T | 1 | a0001c0001t0024g0305 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1494-323C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414972 | ||||||
chr21:36414975
|
T | C | 1 | a0001c0001t0006g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1494-320T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414975 | ||||||
chr21:36415022
|
C | T | 6 | a0001c0001t0008g0043a0001c0001t0008g0044a0001c0001t0008g0045others(3): Show | 6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494-273C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36415022 | ||||||
chr21:36415057
|
G | A | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1494-238G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36415057 | ||||||
chr21:36415147
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1494-148A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36415147 | ||||||
chr21:36415493
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1588+104G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415493 | ||||||
chr21:36415515
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0109a0001c0001t0001g0154others(1): Show | 4 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1588+126C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415515 | ||||||
chr21:36415705
|
T | C | 1 | a0001c0001t0007g0070 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1588+316T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415705 | ||||||
chr21:36415792
|
G | A | 1 | a0001c0008t0001g0198 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1588+403G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415792 | ||||||
chr21:36416001
|
G | A | 1 | a0001c0001t0010g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1589-274G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36416001 | ||||||
chr21:36416049
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1589-226C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36416049 | ||||||
chr21:36416239
|
A | G | 3 | a0001c0001t0022g0328a0001c0001t0025g0052a0001c0001t0026g0051 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1589-36A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36416239 |