geneid | 66005 |
---|---|
ensemblid | ENSG00000177830.18 |
hgncid | 28474 |
symbol | CHID1 |
name | chitinase domain containing 1 |
refseq_nuc | NM_023947.4 |
refseq_prot | NP_076436.3 |
ensembl_nuc | ENST00000323578.13 |
ensembl_prot | ENSP00000325055.8 |
mane_status | MANE Select |
chr | chr11 |
start | 867859 |
end | 910810 |
strand | - |
ver | v1.2 |
region | chr11:867859-910810 |
region5000 | chr11:862859-915810 |
regionname0 | CHID1_chr11_867859_910810 |
regionname5000 | CHID1_chr11_862859_915810 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 393 | 213 | 43 | 24 | 109 | 7 | 30 | 76 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002 | 1/0 | 393 | 160 | 43 | 42 | 57 | 7 | 10 | 44 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0003 | 0/1 | 393 | 10 | 0 | 7 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0004 | 0/0 | 393 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0005 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1182 | 212 | 42 | 24 | 109 | 7 | 30 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0002 | 1/0 | 1182 | 157 | 40 | 42 | 57 | 7 | 10 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0003 | 0/1 | 1182 | 10 | 0 | 7 | 0 | 2 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0004 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0005 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0006 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0007 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0008 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
c0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2079 | 320 | 68 | 65 | 145 | 12 | 30 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0002 | 0/1 | 2079 | 31 | 3 | 8 | 11 | 3 | 5 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0003 | 0/0 | 2079 | 3 | 3 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0004 | 0/0 | 2079 | 2 | 1 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0005 | 0/0 | 2079 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0006 | 0/0 | 2079 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0007 | 0/0 | 2079 | 2 | 0 | 0 | 0 | 1 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0008 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0009 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0010 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0011 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0012 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0013 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0014 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0015 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0016 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0017 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0018 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0019 | 0/0 | 2054 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0020 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0021 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0022 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0023 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0024 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0025 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0026 | 1/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0027 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0028 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0029 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0030 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
t0031 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0005 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1182 | 212 | 42 | 24 | 109 | 7 | 30 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0008 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002 | 1/0 | 1182 | 157 | 40 | 42 | 57 | 7 | 10 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0005 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0006 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0007 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0003c0003 | 0/1 | 1182 | 10 | 0 | 7 | 0 | 2 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0004c0004 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0005c0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3260 | 170 | 32 | 20 | 93 | 4 | 21 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0002 | 0/0 | 3260 | 23 | 3 | 3 | 11 | 2 | 4 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0003 | 0/0 | 3260 | 3 | 3 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0004 | 0/0 | 3260 | 2 | 1 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0007 | 0/0 | 3260 | 2 | 0 | 0 | 0 | 1 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0009 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0013 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0016 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0017 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0019 | 0/0 | 3235 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0021 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0022 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0023 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0028 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0029 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0030 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0001t0031 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0001c0008t0001 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0001 | 0/0 | 3260 | 143 | 33 | 42 | 52 | 7 | 9 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0002 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0005 | 0/0 | 3260 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0008 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0010 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0011 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0012 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0014 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0015 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0018 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0020 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0024 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0026 | 1/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0002t0027 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0005t0025 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0006t0006 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0002c0007t0006 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0003c0003t0001 | 0/0 | 3260 | 3 | 0 | 2 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0003c0003t0002 | 0/1 | 3260 | 7 | 0 | 5 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0004c0004t0001 | 0/0 | 3260 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
a0005c0009t0001 | 0/0 | 3260 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | copy fasta | chr11 | 862859 | 915810 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0019g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0021g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0022g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0023g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0028g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0029g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0030g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0001t0031g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0001c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0001 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0015g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0018g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0024g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0026g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0002t0027g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0005t0025g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0006t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0002c0007t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0004c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
a0005c0009t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0001 | g0153 | EUR | GBR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0215 | EUR | GBR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0013 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00438 | hp2 | a0001 | c0001 | t0023 | g0151 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00558 | hp2 | a0002 | c0002 | t0005 | g0261 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0249 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0096 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0317 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01070 | hp2 | a0003 | c0003 | t0002 | g0158 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01071 | hp1 | a0003 | c0003 | t0002 | g0159 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01106 | hp1 | a0003 | c0003 | t0002 | g0154 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0305 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01109 | hp1 | a0003 | c0003 | t0002 | g0036 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0152 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01243 | hp2 | a0005 | c0009 | t0001 | g0087 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0321 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0292 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0250 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0313 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0276 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01516 | hp1 | a0003 | c0003 | t0002 | g0161 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01884 | hp2 | a0002 | c0002 | t0020 | g0085 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02040 | hp2 | a0002 | c0002 | t0015 | g0082 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02071 | hp2 | a0002 | c0002 | t0008 | g0194 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02129 | hp2 | a0001 | c0001 | t0031 | g0329 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02145 | hp2 | a0002 | c0002 | t0024 | g0270 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02258 | hp2 | a0002 | c0002 | t0012 | g0047 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0186 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02572 | hp1 | a0002 | c0002 | t0014 | g0068 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02615 | hp2 | a0001 | c0001 | t0019 | g0048 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02630 | hp2 | a0001 | c0008 | t0001 | g0138 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02683 | hp1 | a0001 | c0001 | t0022 | g0176 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02738 | hp1 | a0001 | c0001 | t0028 | g0184 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0316 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02965 | hp1 | a0002 | c0002 | t0010 | g0236 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02976 | hp2 | a0004 | c0004 | t0001 | g0318 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03130 | hp2 | a0002 | c0005 | t0025 | g0237 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03139 | hp2 | a0002 | c0007 | t0006 | g0123 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03225 | hp2 | a0002 | c0002 | t0018 | g0049 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0080 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03579 | hp1 | a0002 | c0002 | t0011 | g0302 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03654 | hp1 | a0001 | c0001 | t0007 | g0120 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04184 | hp2 | a0001 | c0001 | t0009 | g0255 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04199 | hp1 | a0001 | c0001 | t0013 | g0041 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18952 | hp2 | a0002 | c0002 | t0027 | g0257 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18957 | hp1 | a0001 | c0001 | t0021 | g0103 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18971 | hp1 | a0001 | c0001 | t0030 | g0330 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19043 | hp2 | a0002 | c0006 | t0006 | g0124 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19064 | hp1 | a0002 | c0002 | t0005 | g0299 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19074 | hp2 | a0001 | c0001 | t0029 | g0187 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ASW | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0315 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0286 | SAS | GIH | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
NA21309 | hp2 | a0004 | c0004 | t0001 | g0038 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0002 | g0160 | REF | REF | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0026 | g0241 | REF | REF | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:870446
|
G | A | 3 | a0001a0003a0004 | 225 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(222): Show |
missense_variant | MODERATE | c.1013C>T | p.Ala338Val | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/13 | 1092/3260 | 1013/1182 | 338/393 | chr11 | 870446 | ||
chr11:870467
|
C | T | 1 | a0003 | 10 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(7): Show |
missense_variant | MODERATE | c.992G>A | p.Arg331Gln | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/13 | 1071/3260 | 992/1182 | 331/393 | chr11 | 870467 | ||
chr11:903039
|
G | A | 1 | a0004 | 2 | HG02976.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.184C>T | p.Leu62Phe | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/13 | 263/3260 | 184/1182 | 62/393 | chr11 | 903039 | ||
chr11:903048
|
T | C | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.175A>G | p.Ser59Gly | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/13 | 254/3260 | 175/1182 | 59/393 | chr11 | 903048 | ||
chr11:904857
|
G | A | 1 | a0001 | 1 | NA19074.hp2 | splice_region_variant | LOW | c.-41C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/13 | chr11 | 904857 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:870136
|
G | A | 2 | a0002c0006a0002c0007 | 2 | HG03139.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1068C>T | p.Phe356Phe | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/13 | 1147/3260 | 1068/1182 | 356/393 | chr11 | 870136 | ||
chr11:870486
|
G | A | 1 | a0002c0007 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.973C>T | p.Leu325Leu | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/13 | 1052/3260 | 973/1182 | 325/393 | chr11 | 870486 | ||
chr11:883264
|
G | A | 1 | a0001c0008 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.843C>T | p.Cys281Cys | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/13 | 922/3260 | 843/1182 | 281/393 | chr11 | 883264 | ||
chr11:903070
|
C | G | 1 | a0002c0005 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.153G>C | p.Val51Val | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/13 | 232/3260 | 153/1182 | 51/393 | chr11 | 903070 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:868139
|
ACCACCCT others(18): Show |
A | 1 | a0001c0001t0019 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1694_*1718delGGGA others(21): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1694 | chr11 | 868139 | |||||
chr11:868226
|
A | G | 1 | a0002c0002t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1632 | chr11 | 868226 | |||||
chr11:868265
|
C | A | 1 | a0002c0002t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1593G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1593 | chr11 | 868265 | |||||
chr11:868303
|
T | C | 1 | a0001c0001t0021 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1555A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1555 | chr11 | 868303 | |||||
chr11:868304
|
C | G | 1 | a0002c0002t0005 | 2 | HG00558.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1554G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1554 | chr11 | 868304 | |||||
chr11:868385
|
T | G | 1 | a0001c0001t0023 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1473A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1473 | chr11 | 868385 | |||||
chr11:868402
|
A | T | 1 | a0002c0005t0025 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1456 | chr11 | 868402 | |||||
chr11:868411
|
A | C | 1 | a0001c0001t0004 | 2 | HG01243.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1447T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1447 | chr11 | 868411 | |||||
chr11:868419
|
G | T | 1 | a0001c0001t0017 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1439C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1439 | chr11 | 868419 | |||||
chr11:868502
|
G | A | 1 | a0001c0001t0022 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1356C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1356 | chr11 | 868502 | |||||
chr11:868533
|
G | A | 1 | a0001c0001t0003 | 3 | HG02055.hp1 HG03209.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1325C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1325 | chr11 | 868533 | |||||
chr11:868654
|
C | G | 1 | a0002c0002t0015 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1204G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1204 | chr11 | 868654 | |||||
chr11:868706
|
C | T | 1 | a0001c0001t0016 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1152 | chr11 | 868706 | |||||
chr11:868727
|
C | A | 2 | a0002c0006t0006a0002c0007t0006 | 2 | HG03139.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1131G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1131 | chr11 | 868727 | |||||
chr11:868740
|
C | T | 1 | a0002c0002t0015 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1118 | chr11 | 868740 | |||||
chr11:868865
|
G | A | 1 | a0001c0001t0023 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 993 | chr11 | 868865 | |||||
chr11:869119
|
G | A | 1 | a0002c0002t0024 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 739 | chr11 | 869119 | |||||
chr11:869158
|
C | T | 4 | a0001c0001t0002a0001c0001t0029a0002c0002t0002others(1): Show | 32 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*700G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 700 | chr11 | 869158 | |||||
chr11:869159
|
G | A | 1 | a0001c0001t0007 | 2 | HG00140.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 699 | chr11 | 869159 | |||||
chr11:869253
|
C | G | 1 | a0002c0002t0014 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 605 | chr11 | 869253 | |||||
chr11:869280
|
C | T | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 578 | chr11 | 869280 | |||||
chr11:869311
|
C | T | 1 | a0001c0001t0013 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 547 | chr11 | 869311 | |||||
chr11:869315
|
C | T | 1 | a0002c0002t0012 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 543 | chr11 | 869315 | |||||
chr11:869360
|
C | T | 1 | a0002c0002t0011 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 498 | chr11 | 869360 | |||||
chr11:869424
|
C | T | 1 | a0002c0002t0010 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*434G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 434 | chr11 | 869424 | |||||
chr11:869444
|
G | C | 1 | a0001c0001t0031 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 414 | chr11 | 869444 | |||||
chr11:869471
|
G | A | 1 | a0002c0002t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 387 | chr11 | 869471 | |||||
chr11:869641
|
G | C | 1 | a0001c0001t0028 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 217 | chr11 | 869641 | |||||
chr11:869724
|
G | T | 1 | a0001c0001t0009 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 134 | chr11 | 869724 | |||||
chr11:869796
|
C | T | 1 | a0002c0002t0008 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 62 | chr11 | 869796 | |||||
chr11:910797
|
G | A | 2 | a0001c0001t0030a0001c0001t0031 | 2 | HG02129.hp2 NA18971.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/13 | chr11 | 910797 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:869959
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02683.hp2 | splice_region_variant&intron_variant | LOW | c.1084-3C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 869959 | ||||||
chr11:869977
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1084-21C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 869977 | ||||||
chr11:870001
|
C | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0199 | 3 | HG02015.hp2 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1084-45G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870001 | ||||||
chr11:870074
|
C | T | 1 | a0002c0002t0001g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1083+47G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870074 | ||||||
chr11:870094
|
CG | C | 6 | a0001c0001t0001g0091a0002c0002t0001g0015a0002c0002t0001g0076others(3): Show | 7 | HG00738.hp1 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+26delC | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870094 | ||||||
chr11:870095
|
G | A | 29 | a0001c0001t0001g0162a0001c0001t0002g0019a0001c0001t0002g0025others(26): Show | 32 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1083+26C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870095 | ||||||
chr11:870237
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041-74G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870237 | ||||||
chr11:870316
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0097 | 3 | NA19004.hp2 NA19065.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1040+103C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870316 | ||||||
chr11:870389
|
A | G | 8 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0084others(5): Show | 10 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1040+30T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870389 | ||||||
chr11:870400
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0003g0017a0001c0001t0003g0075others(2): Show | 6 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+19G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870400 | ||||||
chr11:870401
|
G | A | 8 | a0002c0002t0001g0006a0002c0002t0001g0071a0002c0002t0001g0084others(5): Show | 10 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1040+18C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870401 | ||||||
chr11:870524
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(112): Show | 135 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.960-25C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870524 | ||||||
chr11:870660
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.960-161G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870660 | ||||||
chr11:870722
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.960-223C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870722 | ||||||
chr11:870812
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.960-313G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870812 | ||||||
chr11:870930
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.960-431C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870930 | ||||||
chr11:870966
|
G | A | 1 | a0002c0002t0001g0208 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.960-467C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870966 | ||||||
chr11:870989
|
CT | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.960-491delA | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870989 | ||||||
chr11:871014
|
GGAGTCTC others(1125): Show |
G | 1 | a0001c0001t0001g0168 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.960-1647_960-516de others(1): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871014 | ||||||
chr11:871030
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0130a0001c0001t0001g0133others(5): Show | 11 | HG00735.hp1 HG00741.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.960-531C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871030 | ||||||
chr11:871049
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-550G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871049 | ||||||
chr11:871092
|
G | A | 1 | a0002c0002t0001g0245 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.960-593C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871092 | ||||||
chr11:871183
|
C | T | 1 | a0001c0001t0019g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.960-684G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871183 | ||||||
chr11:871203
|
A | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-704T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871203 | ||||||
chr11:871227
|
G | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-728C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871227 | ||||||
chr11:871238
|
G | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-739C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871238 | ||||||
chr11:871328
|
G | A | 1 | a0002c0002t0001g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.960-829C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871328 | ||||||
chr11:871531
|
A | AGAACACT others(39): Show |
311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.960-1033_960-1032i others(48): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871531 | ||||||
chr11:871531
|
A | AGAACACT others(39): Show |
1 | a0002c0007t0006g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.960-1033_960-1032i others(48): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871531 | ||||||
chr11:871531
|
A | AGAACACT others(39): Show |
15 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0039others(12): Show | 17 | HG00741.hp1 HG01884.hp1 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.960-1033_960-1032i others(48): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871531 | ||||||
chr11:871582
|
C | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.960-1083G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871582 | ||||||
chr11:871591
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.960-1092T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871591 | ||||||
chr11:871689
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.960-1190A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871689 | ||||||
chr11:871703
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.960-1204T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871703 | ||||||
chr11:871742
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.960-1243G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871742 | ||||||
chr11:871759
|
C | T | 1 | a0002c0002t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.960-1260G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871759 | ||||||
chr11:871826
|
C | CGGT | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-1328_960-1327i others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871826 | ||||||
chr11:872059
|
GGAGGCTG others(14): Show |
G | 1 | a0002c0002t0001g0312 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.960-1581_960-1561d others(23): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872059 | ||||||
chr11:872108
|
G | T | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-1609C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872108 | ||||||
chr11:872135
|
C | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0107 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.960-1636G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872135 | ||||||
chr11:872314
|
C | T | 1 | a0002c0002t0001g0284 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.960-1815G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872314 | ||||||
chr11:872408
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0023others(9): Show | 19 | HG00621.hp1 NA18947.hp1 NA18948.hp2 others(16): Show |
intron_variant | MODIFIER | c.960-1909G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872408 | ||||||
chr11:872459
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.960-1960A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872459 | ||||||
chr11:872529
|
C | T | 88 | a0001c0001t0001g0192a0001c0001t0009g0255a0002c0002t0001g0001others(85): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.960-2030G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872529 | ||||||
chr11:872808
|
G | A | 10 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(7): Show | 12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.960-2309C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872808 | ||||||
chr11:872922
|
C | T | 1 | a0004c0004t0001g0318 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.960-2423G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872922 | ||||||
chr11:872992
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.960-2493C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872992 | ||||||
chr11:873223
|
C | G | 1 | a0002c0002t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.960-2724G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873223 | ||||||
chr11:873482
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.960-2983C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873482 | ||||||
chr11:873556
|
G | A | 2 | a0001c0001t0003g0017a0001c0001t0003g0075 | 3 | HG02055.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.960-3057C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873556 | ||||||
chr11:873593
|
G | C | 1 | a0001c0001t0001g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.960-3094C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873593 | ||||||
chr11:873595
|
C | T | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.960-3096G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873595 | ||||||
chr11:873711
|
G | A | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-3212C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873711 | ||||||
chr11:873716
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.960-3217T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873716 | ||||||
chr11:873771
|
C | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 265 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.960-3272G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873771 | ||||||
chr11:873962
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.960-3463C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873962 | ||||||
chr11:873980
|
GGA | G | 11 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(8): Show | 13 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.960-3483_960-3482d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873980 | ||||||
chr11:874038
|
T | G | 3 | a0001c0001t0019g0048a0002c0002t0001g0198a0002c0002t0010g0236 | 3 | HG02615.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.960-3539A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874038 | ||||||
chr11:874160
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960-3661G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874160 | ||||||
chr11:874184
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0147a0001c0001t0023g0151 | 3 | HG00438.hp2 NA18612.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.960-3685C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874184 | ||||||
chr11:874189
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.960-3690A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874189 | ||||||
chr11:874291
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.960-3792T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874291 | ||||||
chr11:874305
|
T | C | 4 | a0002c0002t0001g0050a0002c0002t0001g0063a0002c0002t0001g0064others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-3806A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874305 | ||||||
chr11:874350
|
C | A | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-3851G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874350 | ||||||
chr11:874442
|
G | A | 1 | a0002c0002t0001g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.960-3943C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874442 | ||||||
chr11:874499
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.960-4000C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874499 | ||||||
chr11:874501
|
C | T | 40 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(37): Show | 49 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.960-4002G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874501 | ||||||
chr11:874776
|
G | A | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(36): Show | 48 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.960-4277C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874776 | ||||||
chr11:874935
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-4436G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874935 | ||||||
chr11:874960
|
C | T | 1 | a0002c0002t0001g0250 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.960-4461G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874960 | ||||||
chr11:875117
|
G | A | 329 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(326): Show | 385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.960-4618C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875117 | ||||||
chr11:875500
|
C | A | 1 | a0001c0001t0019g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.960-5001G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875500 | ||||||
chr11:875549
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-5050C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875549 | ||||||
chr11:875591
|
C | G | 1 | a0002c0002t0001g0290 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.960-5092G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875591 | ||||||
chr11:875619
|
G | A | 2 | a0004c0004t0001g0038a0004c0004t0001g0318 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.960-5120C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875619 | ||||||
chr11:875689
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-5190G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875689 | ||||||
chr11:875825
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.960-5326G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875825 | ||||||
chr11:875834
|
A | G | 1 | a0002c0002t0001g0297 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.960-5335T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875834 | ||||||
chr11:875843
|
C | G | 1 | a0002c0002t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.960-5344G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875843 | ||||||
chr11:875981
|
G | A | 1 | a0002c0002t0008g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.960-5482C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875981 | ||||||
chr11:876028
|
C | CG | 3 | a0001c0001t0002g0199a0002c0002t0001g0213a0002c0002t0001g0235 | 3 | HG02080.hp2 HG02257.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.960-5530dupC | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876028 | ||||||
chr11:876148
|
G | T | 1 | a0002c0002t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.960-5649C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876148 | ||||||
chr11:876245
|
C | T | 3 | a0002c0002t0001g0291a0002c0002t0001g0292a0002c0002t0002g0155 | 3 | HG01256.hp2 HG01258.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.960-5746G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876245 | ||||||
chr11:876582
|
C | A | 2 | a0002c0006t0006g0124a0002c0007t0006g0123 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.960-6083G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876582 | ||||||
chr11:876624
|
T | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 241 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.960-6125A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876624 | ||||||
chr11:876707
|
C | T | 13 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(10): Show | 15 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.960-6208G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876707 | ||||||
chr11:876715
|
C | T | 1 | a0001c0001t0001g0021 | 2 | NA18959.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.960-6216G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876715 | ||||||
chr11:876755
|
T | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 241 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.960-6256A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876755 | ||||||
chr11:877394
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.959+5754G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877394 | ||||||
chr11:877406
|
C | T | 1 | a0003c0003t0002g0154 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.959+5742G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877406 | ||||||
chr11:877560
|
T | C | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.959+5588A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877560 | ||||||
chr11:877596
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+5552G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877596 | ||||||
chr11:877717
|
T | TGGCACTG others(25): Show |
1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+5399_959+5430d others(34): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877717 | ||||||
chr11:877717
|
T | TGGCACTG others(57): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0051a0002c0002t0001g0079 | 4 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+5367_959+5430d others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877717 | ||||||
chr11:877750
|
G | A | 1 | a0002c0002t0001g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.959+5398C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877750 | ||||||
chr11:877783
|
G | GCACTGTG others(25): Show |
27 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(24): Show | 29 | HG00140.hp1 HG00544.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.959+5333_959+5364d others(34): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | ||||||
chr11:877783
|
G | GCACTGTG others(57): Show |
7 | a0001c0001t0002g0027a0001c0001t0002g0094a0001c0001t0002g0172others(4): Show | 8 | HG02015.hp2 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+5364_959+5365i others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | ||||||
chr11:877783
|
G | GCACTGTG others(57): Show |
13 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(10): Show | 15 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.959+5364_959+5365i others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | ||||||
chr11:877783
|
G | GCACTGTG others(57): Show |
150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.959+5364_959+5365i others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | ||||||
chr11:877815
|
A | ACACTGTG others(153): Show |
1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+5332_959+5333i others(162): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877815 | ||||||
chr11:877847
|
G | A | 126 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(123): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.959+5301C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877847 | ||||||
chr11:877869
|
T | C | 1 | a0002c0002t0001g0297 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.959+5279A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877869 | ||||||
chr11:877869
|
T | TTAGAAGG others(25): Show |
126 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(123): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.959+5278_959+5279i others(34): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877869 | ||||||
chr11:878151
|
C | T | 1 | a0002c0002t0001g0191 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.959+4997G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878151 | ||||||
chr11:878226
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.959+4922G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878226 | ||||||
chr11:878253
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0145 | 3 | HG01934.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.959+4895T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878253 | ||||||
chr11:878301
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.959+4847G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878301 | ||||||
chr11:878372
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0137others(1): Show | 7 | HG02280.hp1 HG02630.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+4776G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878372 | ||||||
chr11:878427
|
G | A | 1 | a0002c0002t0001g0277 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.959+4721C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878427 | ||||||
chr11:878488
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.959+4660T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878488 | ||||||
chr11:878562
|
TA | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0135a0002c0002t0001g0229others(4): Show | 7 | HG01070.hp2 HG02965.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+4585delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878562 | ||||||
chr11:878598
|
TCA | T | 2 | a0002c0002t0001g0031a0002c0002t0001g0276 | 3 | HG00733.hp1 HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.959+4548_959+4549d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878598 | ||||||
chr11:878634
|
G | A | 1 | a0002c0002t0024g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.959+4514C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878634 | ||||||
chr11:878848
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+4300C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878848 | ||||||
chr11:878858
|
T | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0145 | 3 | HG01934.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.959+4290A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878858 | ||||||
chr11:878859
|
T | A | 1 | a0001c0001t0019g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.959+4289A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878859 | ||||||
chr11:879003
|
C | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(7): Show | 12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+4145G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879003 | ||||||
chr11:879081
|
T | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 241 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.959+4067A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879081 | ||||||
chr11:879125
|
T | C | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+4023A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879125 | ||||||
chr11:879142
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.959+4006C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879142 | ||||||
chr11:879375
|
T | C | 1 | a0002c0002t0001g0316 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.959+3773A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879375 | ||||||
chr11:879497
|
G | GGGAGAAG others(77): Show |
198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 238 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.959+3650_959+3651i others(86): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879497 | ||||||
chr11:879497
|
G | GGGAGAAG others(77): Show |
1 | a0001c0001t0001g0314 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.959+3650_959+3651i others(86): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879497 | ||||||
chr11:879497
|
G | GGGAGAAG others(77): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.959+3650_959+3651i others(86): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879497 | ||||||
chr11:879508
|
G | C | 1 | a0002c0002t0001g0316 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.959+3640C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879508 | ||||||
chr11:879587
|
C | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(7): Show | 12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+3561G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879587 | ||||||
chr11:879691
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+3457C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879691 | ||||||
chr11:879820
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.959+3328A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879820 | ||||||
chr11:879921
|
G | A | 2 | a0001c0001t0007g0120a0001c0001t0007g0215 | 2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.959+3227C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879921 | ||||||
chr11:880069
|
C | G | 2 | a0001c0001t0001g0091a0002c0002t0024g0270 | 2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.959+3079G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880069 | ||||||
chr11:880103
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.959+3045G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880103 | ||||||
chr11:880172
|
G | A | 2 | a0004c0004t0001g0038a0004c0004t0001g0318 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.959+2976C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880172 | ||||||
chr11:880178
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+2970C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880178 | ||||||
chr11:880272
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | HG01069.hp1 HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.959+2876G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880272 | ||||||
chr11:880318
|
C | T | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.959+2830G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880318 | ||||||
chr11:880419
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 99 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.959+2729G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880419 | ||||||
chr11:880461
|
A | T | 1 | a0002c0002t0001g0032 | 2 | HG01255.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.959+2687T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880461 | ||||||
chr11:880467
|
G | A | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.959+2681C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880467 | ||||||
chr11:880705
|
C | T | 1 | a0002c0002t0024g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.959+2443G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880705 | ||||||
chr11:880847
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.959+2301A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880847 | ||||||
chr11:881117
|
C | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.959+2031G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881117 | ||||||
chr11:881182
|
G | A | 1 | a0002c0002t0001g0245 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.959+1966C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881182 | ||||||
chr11:881184
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.959+1964C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881184 | ||||||
chr11:881191
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.959+1957G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881191 | ||||||
chr11:881277
|
T | C | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1871A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881277 | ||||||
chr11:881286
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.959+1862T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881286 | ||||||
chr11:881339
|
C | T | 1 | a0002c0002t0001g0227 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.959+1809G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881339 | ||||||
chr11:881369
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.959+1779G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881369 | ||||||
chr11:881420
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1728G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881420 | ||||||
chr11:881441
|
CACGTCGG others(27): Show |
C | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 182 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.959+1673_959+1706d others(36): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881441 | ||||||
chr11:881451
|
G | A | 1 | a0002c0002t0015g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.959+1697C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881451 | ||||||
chr11:881457
|
CTGGGTGG others(101): Show |
C | 2 | a0001c0001t0001g0028a0001c0001t0001g0112 | 3 | HG03490.hp2 HG03492.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.959+1583_959+1690d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881457 | ||||||
chr11:881457
|
CTGGGTGG others(138): Show |
C | 28 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(25): Show | 31 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.959+1546_959+1690d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881457 | ||||||
chr11:881475
|
G | GACC | 20 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0091others(17): Show | 22 | HG00597.hp1 HG01070.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(33): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0183 | 2 | NA18978.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.959+1672_959+1673i others(42): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(70): Show |
1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1672_959+1673i others(79): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(70): Show |
10 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 12 | HG01361.hp2 HG02071.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(79): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(107): Show |
3 | a0002c0002t0001g0208a0002c0002t0001g0279a0002c0002t0001g0319 | 3 | HG00609.hp1 HG01928.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.959+1672_959+1673i others(116): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(144): Show |
8 | a0002c0002t0001g0196a0002c0002t0001g0223a0002c0002t0001g0224others(5): Show | 8 | HG00673.hp1 NA18945.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(153): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(181): Show |
62 | a0001c0001t0001g0192a0001c0001t0009g0255a0002c0002t0001g0001others(59): Show | 73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(190): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(218): Show |
38 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0269others(35): Show | 42 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(227): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881475
|
G | GACCACGT others(255): Show |
5 | a0002c0002t0001g0222a0002c0002t0001g0242a0002c0002t0001g0288others(2): Show | 5 | HG01167.hp2 HG02273.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(264): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | ||||||
chr11:881476
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.959+1672T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881476 | ||||||
chr11:881490
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1658C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881490 | ||||||
chr11:881497
|
G | GGTGAGGG others(141): Show |
1 | a0002c0002t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.959+1650_959+1651i others(150): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881497 | ||||||
chr11:881520
|
G | A | 3 | a0002c0002t0001g0015a0002c0002t0001g0076a0002c0002t0012g0047 | 4 | HG02258.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+1628C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881520 | ||||||
chr11:881528
|
CTGGGTGG others(30): Show |
C | 1 | a0002c0002t0001g0225 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.959+1583_959+1619d others(39): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881528 | ||||||
chr11:881545
|
GGACCACG others(104): Show |
G | 6 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0113others(3): Show | 8 | HG02155.hp1 NA18957.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.959+1492_959+1602d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881545 | ||||||
chr11:881565
|
T | C | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(277): Show | 330 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.959+1583A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881565 | ||||||
chr11:881582
|
GGACCACG others(67): Show |
G | 10 | a0001c0001t0001g0091a0001c0001t0001g0126a0001c0001t0001g0148others(7): Show | 10 | HG00597.hp1 HG01192.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+1492_959+1565d others(76): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881582 | ||||||
chr11:881602
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 335 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.959+1546A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881602 | ||||||
chr11:881639
|
T | C | 153 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0097others(150): Show | 171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.959+1509A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881639 | ||||||
chr11:881647
|
T | TGAGGGAA others(182): Show |
1 | a0002c0002t0001g0227 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.959+1500_959+1501i others(191): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881647 | ||||||
chr11:881651
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 229 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.959+1497T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881651 | ||||||
chr11:881656
|
T | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 225 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.959+1492A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881656 | ||||||
chr11:881998
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.959+1150A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881998 | ||||||
chr11:882003
|
C | CA | 12 | a0001c0001t0001g0018a0001c0001t0001g0060a0001c0001t0001g0095others(9): Show | 13 | HG02027.hp2 HG02055.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.959+1144dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882003 | ||||||
chr11:882003
|
CA | C | 20 | a0001c0001t0001g0067a0001c0001t0001g0100a0001c0001t0001g0101others(17): Show | 20 | HG01070.hp1 HG01255.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.959+1144delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882003 | ||||||
chr11:882003
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0007g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.959+1135_959+1144d others(12): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882003 | ||||||
chr11:882036
|
A | T | 1 | a0002c0002t0001g0293 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.959+1112T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882036 | ||||||
chr11:882049
|
C | T | 1 | a0001c0001t0030g0330 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.959+1099G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882049 | ||||||
chr11:882065
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.959+1083G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882065 | ||||||
chr11:882142
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0137others(1): Show | 7 | HG02280.hp1 HG02630.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+1006G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882142 | ||||||
chr11:882181
|
A | C | 1 | a0002c0002t0001g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.959+967T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882181 | ||||||
chr11:882187
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.959+961G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882187 | ||||||
chr11:882406
|
C | T | 25 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(22): Show | 27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.959+742G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882406 | ||||||
chr11:882455
|
G | C | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+693C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882455 | ||||||
chr11:882558
|
A | C | 3 | a0002c0002t0001g0222a0002c0002t0001g0242a0002c0002t0001g0243 | 3 | HG01167.hp2 HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.959+590T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882558 | ||||||
chr11:882656
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+492C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882656 | ||||||
chr11:882731
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.959+417T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882731 | ||||||
chr11:882755
|
A | G | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.959+393T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882755 | ||||||
chr11:882860
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.959+288A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882860 | ||||||
chr11:882863
|
T | C | 2 | a0002c0002t0001g0267a0002c0002t0001g0268 | 2 | NA18960.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.959+285A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882863 | ||||||
chr11:882900
|
CCAGCCTC others(15): Show |
C | 6 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 8 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+226_959+247del others(22): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882900 | ||||||
chr11:883058
|
G | A | 1 | a0001c0001t0019g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.959+90C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883058 | ||||||
chr11:883079
|
T | A | 2 | a0001c0001t0030g0330a0001c0001t0031g0329 | 2 | HG02129.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.959+69A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883079 | ||||||
chr11:883124
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.959+24G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883124 | ||||||
chr11:883131
|
G | A | 3 | a0002c0002t0001g0015a0002c0002t0001g0076a0002c0002t0012g0047 | 4 | HG02258.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+17C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883131 | ||||||
chr11:883364
|
T | C | 1 | a0002c0002t0015g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.804-61A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883364 | ||||||
chr11:883384
|
G | A | 2 | a0002c0002t0001g0031a0002c0002t0001g0276 | 3 | HG00733.hp1 HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.804-81C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883384 | ||||||
chr11:883391
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.804-88G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883391 | ||||||
chr11:883394
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-91G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883394 | ||||||
chr11:883479
|
G | C | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.804-176C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883479 | ||||||
chr11:883592
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.804-289C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883592 | ||||||
chr11:883606
|
C | A | 1 | a0001c0001t0007g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.804-303G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883606 | ||||||
chr11:883614
|
C | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0106others(2): Show | 7 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.804-311G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883614 | ||||||
chr11:883788
|
G | C | 1 | a0002c0002t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.803+280C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883788 | ||||||
chr11:883843
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803+225G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883843 | ||||||
chr11:883930
|
T | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.803+138A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883930 | ||||||
chr11:884002
|
A | G | 3 | a0002c0002t0001g0291a0002c0002t0001g0292a0002c0002t0001g0304 | 3 | HG00735.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.803+66T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 884002 | ||||||
chr11:884193
|
C | T | 27 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(24): Show | 29 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.702-24G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884193 | ||||||
chr11:884346
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.702-177C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884346 | ||||||
chr11:884369
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.702-200T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884369 | ||||||
chr11:884543
|
T | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 99 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.702-374A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884543 | ||||||
chr11:884743
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.702-574G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884743 | ||||||
chr11:884780
|
C | T | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-611G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884780 | ||||||
chr11:884808
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.702-639C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884808 | ||||||
chr11:884900
|
C | A | 1 | a0002c0002t0001g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.702-731G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884900 | ||||||
chr11:885064
|
G | A | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.702-895C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885064 | ||||||
chr11:885078
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.702-909A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885078 | ||||||
chr11:885189
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.702-1020G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885189 | ||||||
chr11:885253
|
G | A | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-1084C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885253 | ||||||
chr11:885305
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.702-1136G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885305 | ||||||
chr11:885319
|
T | G | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.702-1150A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885319 | ||||||
chr11:885330
|
C | A | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-1161G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885330 | ||||||
chr11:885435
|
C | T | 1 | a0001c0001t0021g0103 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.702-1266G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885435 | ||||||
chr11:885473
|
CA | C | 3 | a0002c0002t0001g0015a0002c0002t0001g0076a0002c0002t0012g0047 | 4 | HG02258.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.702-1305delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885473 | ||||||
chr11:885480
|
G | A | 66 | a0001c0001t0001g0192a0001c0001t0009g0255a0002c0002t0001g0001others(63): Show | 75 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.702-1311C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885480 | ||||||
chr11:885542
|
C | T | 2 | a0002c0002t0001g0248a0002c0002t0001g0298 | 2 | HG01361.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.702-1373G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885542 | ||||||
chr11:885553
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.702-1384A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885553 | ||||||
chr11:885564
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.702-1395A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885564 | ||||||
chr11:885637
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.702-1468G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885637 | ||||||
chr11:885685
|
T | C | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-1516A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885685 | ||||||
chr11:885695
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 238 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.702-1526G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885695 | ||||||
chr11:885716
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0282 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.702-1547G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885716 | ||||||
chr11:885949
|
G | A | 1 | a0002c0002t0001g0276 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.702-1780C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885949 | ||||||
chr11:886145
|
C | T | 1 | a0002c0002t0001g0220 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.702-1976G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886145 | ||||||
chr11:886150
|
C | CA | 5 | a0001c0001t0001g0162a0001c0001t0002g0059a0001c0001t0002g0190others(2): Show | 5 | HG01074.hp1 HG02257.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.702-1982dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886150 | ||||||
chr11:886157
|
AG | A | 148 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0028others(145): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.702-1989delC | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886157 | ||||||
chr11:886158
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 212 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.702-1989C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886158 | ||||||
chr11:886170
|
G | A | 6 | a0001c0001t0001g0056a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-2001C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886170 | ||||||
chr11:886172
|
A | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-2003T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886172 | ||||||
chr11:886176
|
AT | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 177 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.702-2008delA | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886176 | ||||||
chr11:886177
|
T | A | 6 | a0001c0001t0001g0056a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-2008A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886177 | ||||||
chr11:886191
|
G | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0146others(6): Show | 10 | HG00438.hp2 HG00597.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.702-2022C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886191 | ||||||
chr11:886453
|
T | C | 7 | a0002c0002t0001g0081a0002c0002t0001g0277a0002c0002t0001g0278others(4): Show | 7 | HG01070.hp1 HG01346.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.702-2284A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886453 | ||||||
chr11:886690
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0137others(1): Show | 7 | HG02280.hp1 HG02630.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-2521G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886690 | ||||||
chr11:886695
|
C | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0322a0001c0001t0002g0323 | 3 | HG02486.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.702-2526G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886695 | ||||||
chr11:886709
|
C | T | 1 | a0002c0002t0001g0328 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.702-2540G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886709 | ||||||
chr11:886730
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.702-2561C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886730 | ||||||
chr11:886752
|
T | C | 1 | a0002c0002t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702-2583A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886752 | ||||||
chr11:886869
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.702-2700T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886869 | ||||||
chr11:887102
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.702-2933G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887102 | ||||||
chr11:887220
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3051C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887220 | ||||||
chr11:887225
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.702-3056T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887225 | ||||||
chr11:887322
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3153C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887322 | ||||||
chr11:887402
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.702-3233T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887402 | ||||||
chr11:887420
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3251C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887420 | ||||||
chr11:887431
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.702-3262C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887431 | ||||||
chr11:887458
|
G | T | 26 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(23): Show | 28 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.702-3289C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887458 | ||||||
chr11:887560
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG01261.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.702-3391G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887560 | ||||||
chr11:887561
|
C | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3392G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887561 | ||||||
chr11:887741
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.702-3572A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887741 | ||||||
chr11:887977
|
C | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3808G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887977 | ||||||
chr11:888068
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0121 | 3 | NA18944.hp1 NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.702-3899C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888068 | ||||||
chr11:888086
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0118 | 2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.702-3917A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888086 | ||||||
chr11:888115
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.702-3946G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888115 | ||||||
chr11:888150
|
T | C | 130 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0091others(127): Show | 146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.702-3981A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888150 | ||||||
chr11:888187
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.702-4018C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888187 | ||||||
chr11:888188
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.702-4019T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888188 | ||||||
chr11:888339
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.702-4170A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888339 | ||||||
chr11:888533
|
G | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 238 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.702-4364C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888533 | ||||||
chr11:888632
|
G | A | 129 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0091others(126): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.702-4463C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888632 | ||||||
chr11:888716
|
C | G | 1 | a0001c0001t0028g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.702-4547G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888716 | ||||||
chr11:888740
|
T | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.702-4571A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888740 | ||||||
chr11:888759
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.702-4590G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888759 | ||||||
chr11:888760
|
G | A | 1 | a0002c0002t0001g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.702-4591C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888760 | ||||||
chr11:888833
|
T | TGCCAGTG others(91): Show |
1 | a0002c0002t0001g0251 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.701+4593_701+4594i others(100): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888833 | ||||||
chr11:888858
|
G | A | 1 | a0002c0002t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.701+4569C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888858 | ||||||
chr11:888957
|
G | A | 127 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0192others(124): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.701+4470C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888957 | ||||||
chr11:889112
|
C | T | 1 | a0001c0001t0019g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.701+4315G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889112 | ||||||
chr11:889137
|
C | T | 2 | a0002c0002t0001g0223a0002c0002t0001g0224 | 2 | NA18966.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.701+4290G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889137 | ||||||
chr11:889138
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701+4289C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889138 | ||||||
chr11:889690
|
C | A | 1 | a0002c0002t0008g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.701+3737G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889690 | ||||||
chr11:889858
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181 | 3 | HG00621.hp2 HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.701+3569C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889858 | ||||||
chr11:890048
|
C | G | 1 | a0002c0002t0001g0307 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.701+3379G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890048 | ||||||
chr11:890091
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.701+3336C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890091 | ||||||
chr11:890131
|
G | A | 5 | a0001c0001t0001g0029a0002c0002t0001g0271a0002c0002t0001g0272others(2): Show | 6 | HG00642.hp1 HG02258.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.701+3296C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890131 | ||||||
chr11:890197
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(33): Show | 49 | HG00558.hp1 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.701+3230G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890197 | ||||||
chr11:890263
|
C | G | 1 | a0003c0003t0002g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.701+3164G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890263 | ||||||
chr11:890275
|
CCT | C | 5 | a0002c0002t0001g0034a0002c0002t0001g0295a0002c0002t0001g0303others(2): Show | 6 | HG01346.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+3150_701+3151d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890275 | ||||||
chr11:890355
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.701+3072C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890355 | ||||||
chr11:890405
|
T | C | 134 | a0001c0001t0001g0024a0001c0001t0001g0067a0001c0001t0001g0069others(131): Show | 151 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.701+3022A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890405 | ||||||
chr11:890673
|
AC | A | 10 | a0002c0002t0001g0006a0002c0002t0001g0037a0002c0002t0001g0071others(7): Show | 12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+2753delG | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890673 | ||||||
chr11:890779
|
T | G | 2 | a0002c0002t0001g0072a0002c0002t0001g0073 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.701+2648A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890779 | ||||||
chr11:890864
|
A | G | 1 | a0002c0002t0001g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.701+2563T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890864 | ||||||
chr11:890866
|
G | A | 1 | a0002c0002t0001g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.701+2561C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890866 | ||||||
chr11:890906
|
A | G | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+2521T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890906 | ||||||
chr11:890985
|
T | TGCTCTTG others(37): Show |
1 | a0001c0001t0001g0169 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.701+2398_701+2441d others(46): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890985 | ||||||
chr11:891019
|
C | T | 1 | a0002c0002t0001g0285 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.701+2408G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891019 | ||||||
chr11:891094
|
G | A | 2 | a0001c0001t0001g0162a0002c0002t0010g0236 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.701+2333C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891094 | ||||||
chr11:891106
|
A | AAC | 83 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0001g0296others(80): Show | 92 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.701+2319_701+2320d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891106 | ||||||
chr11:891157
|
G | A | 3 | a0002c0002t0001g0281a0002c0006t0006g0124a0002c0007t0006g0123 | 3 | HG03139.hp2 NA19043.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.701+2270C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891157 | ||||||
chr11:891189
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.701+2238G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891189 | ||||||
chr11:891196
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.701+2231C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891196 | ||||||
chr11:891326
|
G | A | 4 | a0002c0002t0001g0230a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | NA18960.hp2 NA19058.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+2101C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891326 | ||||||
chr11:891328
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.701+2099G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891328 | ||||||
chr11:891331
|
C | T | 1 | a0002c0002t0001g0032 | 2 | HG01255.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.701+2096G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891331 | ||||||
chr11:891338
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 197 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.701+2089C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891338 | ||||||
chr11:891384
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+2043C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891384 | ||||||
chr11:891417
|
G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+2010C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891417 | ||||||
chr11:891438
|
T | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0142a0001c0001t0001g0144 | 3 | HG01358.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.701+1989A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891438 | ||||||
chr11:891512
|
G | A | 3 | a0002c0002t0001g0034a0002c0002t0001g0312a0002c0002t0001g0313 | 4 | HG01346.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+1915C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891512 | ||||||
chr11:891571
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(74): Show | 98 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.701+1856G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891571 | ||||||
chr11:891689
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.701+1738C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891689 | ||||||
chr11:891732
|
C | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0106others(2): Show | 7 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.701+1695G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891732 | ||||||
chr11:891734
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.701+1693A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891734 | ||||||
chr11:891853
|
C | T | 26 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(23): Show | 28 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.701+1574G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891853 | ||||||
chr11:891854
|
G | A | 2 | a0002c0002t0001g0315a0002c0002t0001g0317 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.701+1573C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891854 | ||||||
chr11:891938
|
CA | C | 33 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0091others(30): Show | 34 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.701+1488delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | ||||||
chr11:891938
|
CAA | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(227): Show | 274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.701+1487_701+1488d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | ||||||
chr11:891938
|
CAAA | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(30): Show | 42 | HG00558.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.701+1486_701+1488d others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | ||||||
chr11:891938
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.701+1477_701+1488d others(14): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | ||||||
chr11:891953
|
A | G | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+1474T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891953 | ||||||
chr11:891956
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.701+1471T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891956 | ||||||
chr11:891960
|
A | C | 117 | a0001c0001t0001g0091a0001c0001t0001g0192a0001c0001t0001g0269others(114): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.701+1467T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891960 | ||||||
chr11:891970
|
A | C | 1 | a0001c0001t0001g0240 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.701+1457T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891970 | ||||||
chr11:891972
|
T | C | 17 | a0001c0001t0001g0097a0001c0001t0002g0019a0001c0001t0002g0025others(14): Show | 19 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.701+1455A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891972 | ||||||
chr11:891977
|
G | T | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+1450C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891977 | ||||||
chr11:891983
|
A | G | 118 | a0001c0001t0001g0091a0001c0001t0001g0192a0001c0001t0001g0269others(115): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.701+1444T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891983 | ||||||
chr11:892062
|
A | G | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+1365T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892062 | ||||||
chr11:892089
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 222 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.701+1338A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892089 | ||||||
chr11:892095
|
A | T | 1 | a0001c0001t0001g0174 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.701+1332T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892095 | ||||||
chr11:892110
|
A | G | 67 | a0001c0001t0001g0192a0001c0001t0001g0296a0001c0001t0009g0255others(64): Show | 76 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.701+1317T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892110 | ||||||
chr11:892161
|
C | A | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.701+1266G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892161 | ||||||
chr11:892212
|
G | A | 1 | a0002c0002t0001g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.701+1215C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892212 | ||||||
chr11:892327
|
C | T | 1 | a0002c0002t0001g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.701+1100G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892327 | ||||||
chr11:892461
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.701+966A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892461 | ||||||
chr11:892465
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+962G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892465 | ||||||
chr11:892497
|
C | G | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+930G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892497 | ||||||
chr11:892611
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.701+816C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892611 | ||||||
chr11:892648
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.701+779G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892648 | ||||||
chr11:892760
|
A | G | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.701+667T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892760 | ||||||
chr11:892766
|
G | C | 2 | a0001c0001t0001g0091a0002c0002t0024g0270 | 2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.701+661C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892766 | ||||||
chr11:893152
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.701+275C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 893152 | ||||||
chr11:893299
|
T | C | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.701+128A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 893299 | ||||||
chr11:893417
|
C | T | 1 | a0002c0002t0001g0307 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.701+10G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 893417 | ||||||
chr11:893588
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.609-69G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893588 | ||||||
chr11:893708
|
GC | G | 25 | a0001c0001t0001g0097a0001c0001t0002g0019a0001c0001t0002g0025others(22): Show | 27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.609-190delG | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893708 | ||||||
chr11:893715
|
T | C | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609-196A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893715 | ||||||
chr11:893872
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.609-353G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893872 | ||||||
chr11:893925
|
C | T | 2 | a0002c0002t0001g0035a0002c0002t0001g0254 | 3 | HG00639.hp1 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.609-406G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893925 | ||||||
chr11:893928
|
C | CTTGGCCA others(31): Show |
1 | a0001c0001t0001g0327 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.609-447_609-410dup others(38): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893928 | ||||||
chr11:893984
|
T | C | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.609-465A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893984 | ||||||
chr11:894058
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.609-539C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894058 | ||||||
chr11:894121
|
CA | C | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 98 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.609-603delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | ||||||
chr11:894121
|
CAA | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 101 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.609-604_609-603del others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | ||||||
chr11:894121
|
CAAA | C | 97 | a0001c0001t0001g0022a0001c0001t0001g0127a0001c0001t0001g0128others(94): Show | 114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.609-605_609-603del others(3): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | ||||||
chr11:894121
|
CAAAAAA | C | 4 | a0001c0001t0003g0017a0001c0001t0003g0075a0002c0002t0001g0015others(1): Show | 6 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.609-608_609-603del others(6): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | ||||||
chr11:894121
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0051others(4): Show | 7 | HG02074.hp2 HG02129.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.609-612_609-603del others(10): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | ||||||
chr11:894121
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0044 | 4 | HG02004.hp2 HG04228.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-618_609-603del others(16): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | ||||||
chr11:894132
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0099 | 2 | HG02486.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.609-613T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894132 | ||||||
chr11:894132
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.609-613T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894132 | ||||||
chr11:894133
|
A | G | 21 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(18): Show | 23 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.609-614T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894133 | ||||||
chr11:894134
|
A | G | 3 | a0003c0003t0001g0152a0003c0003t0001g0153a0003c0003t0002g0154 | 3 | HG00140.hp1 HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.609-615T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894134 | ||||||
chr11:894205
|
T | C | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.609-686A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894205 | ||||||
chr11:894832
|
A | C | 1 | a0002c0002t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.609-1313T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894832 | ||||||
chr11:894874
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 222 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.609-1355T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894874 | ||||||
chr11:894885
|
C | A | 1 | a0002c0002t0001g0037 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.609-1366G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894885 | ||||||
chr11:895014
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.609-1495G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895014 | ||||||
chr11:895070
|
C | T | 1 | a0002c0002t0001g0308 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.609-1551G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895070 | ||||||
chr11:895144
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.609-1625C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895144 | ||||||
chr11:895176
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.609-1657T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895176 | ||||||
chr11:895453
|
G | T | 1 | a0002c0002t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.609-1934C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895453 | ||||||
chr11:895490
|
C | T | 2 | a0002c0002t0001g0315a0002c0002t0001g0317 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.609-1971G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895490 | ||||||
chr11:895596
|
C | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 60 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.609-2077G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895596 | ||||||
chr11:895744
|
C | G | 116 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(113): Show | 132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.609-2225G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895744 | ||||||
chr11:895792
|
G | A | 1 | a0002c0002t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.609-2273C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895792 | ||||||
chr11:895881
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.609-2362C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895881 | ||||||
chr11:895982
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.609-2463A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895982 | ||||||
chr11:896025
|
C | T | 2 | a0001c0001t0001g0091a0002c0002t0024g0270 | 2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.609-2506G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896025 | ||||||
chr11:896081
|
C | T | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.609-2562G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896081 | ||||||
chr11:896082
|
GCAGCCTC others(619): Show |
G | 7 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+2632_609-2564d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896082 | ||||||
chr11:896143
|
G | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609-2624C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896143 | ||||||
chr11:896275
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.609-2756G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896275 | ||||||
chr11:896300
|
C | G | 17 | a0002c0002t0001g0005a0002c0002t0001g0035a0002c0002t0001g0193others(14): Show | 21 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.609-2781G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896300 | ||||||
chr11:896459
|
AAGGCTGT others(31): Show |
A | 2 | a0002c0002t0001g0037a0002c0002t0001g0198 | 2 | HG01943.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.608+2843_608+2880d others(40): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896459 | ||||||
chr11:896495
|
ATGAGGCT others(31): Show |
A | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0002c0002t0001g0247 | 3 | HG03710.hp2 HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.608+2807_608+2844d others(40): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896495 | ||||||
chr11:896496
|
T | C | 114 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(111): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.608+2844A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896496 | ||||||
chr11:896532
|
C | T | 1 | a0002c0002t0001g0306 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.608+2808G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896532 | ||||||
chr11:896534
|
T | C | 1 | a0002c0002t0001g0247 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.608+2806A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896534 | ||||||
chr11:896548
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | HG01069.hp1 HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.608+2792G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896548 | ||||||
chr11:896553
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.608+2787G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896553 | ||||||
chr11:896587
|
ACCCCCAG others(34): Show |
A | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.608+2712_608+2752d others(43): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896587 | ||||||
chr11:896718
|
C | G | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.608+2622G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896718 | ||||||
chr11:896726
|
G | A | 34 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0028others(31): Show | 39 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.608+2614C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896726 | ||||||
chr11:896763
|
C | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(69): Show | 85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.608+2577G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896763 | ||||||
chr11:896806
|
T | C | 1 | a0001c0001t0002g0323 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.608+2534A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896806 | ||||||
chr11:896821
|
G | A | 1 | a0002c0002t0001g0253 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.608+2519C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896821 | ||||||
chr11:896845
|
T | G | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.608+2495A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896845 | ||||||
chr11:896867
|
ACTCCACC others(31): Show |
A | 3 | a0001c0001t0001g0091a0001c0001t0001g0238a0002c0002t0024g0270 | 3 | HG01192.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.608+2435_608+2472d others(40): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896867 | ||||||
chr11:896875
|
C | A | 1 | a0002c0002t0001g0305 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.608+2465G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896875 | ||||||
chr11:896904
|
G | C | 1 | a0001c0001t0016g0080 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.608+2436C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896904 | ||||||
chr11:896911
|
C | CCCCAGAC others(34): Show |
1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.608+2428_608+2429i others(43): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896911 | ||||||
chr11:896918
|
C | CACA | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2421_608+2422i others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896918 | ||||||
chr11:896949
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2391G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896949 | ||||||
chr11:896952
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0074a0002c0002t0001g0079 | 4 | HG02572.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+2388G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896952 | ||||||
chr11:896956
|
CACA | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2381_608+2383d others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896956 | ||||||
chr11:896979
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.608+2361G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896979 | ||||||
chr11:896980
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.608+2360G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896980 | ||||||
chr11:896990
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.608+2350A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896990 | ||||||
chr11:896993
|
C | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2347G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896993 | ||||||
chr11:896995
|
G | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2345C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896995 | ||||||
chr11:896997
|
C | CA | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2342dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896997 | ||||||
chr11:896999
|
C | T | 1 | a0001c0001t0028g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.608+2341G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896999 | ||||||
chr11:897017
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.608+2323G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897017 | ||||||
chr11:897018
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.608+2322G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897018 | ||||||
chr11:897031
|
G | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.608+2309C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897031 | ||||||
chr11:897033
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.608+2307G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897033 | ||||||
chr11:897035
|
CA | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.608+2304delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897035 | ||||||
chr11:897036
|
AACGAGCC others(69): Show |
A | 1 | a0002c0002t0001g0306 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.608+2228_608+2303d others(78): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897036 | ||||||
chr11:897038
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.608+2302G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897038 | ||||||
chr11:897094
|
T | C | 2 | a0001c0001t0001g0144a0003c0003t0002g0036 | 2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.608+2246A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897094 | ||||||
chr11:897095
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.608+2245C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897095 | ||||||
chr11:897114
|
C | T | 1 | a0001c0001t0021g0103 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.608+2226G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897114 | ||||||
chr11:897181
|
C | T | 2 | a0002c0006t0006g0124a0002c0007t0006g0123 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.608+2159G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897181 | ||||||
chr11:897193
|
C | T | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.608+2147G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897193 | ||||||
chr11:897306
|
G | A | 1 | a0001c0001t0023g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.608+2034C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897306 | ||||||
chr11:897589
|
A | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.608+1751T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897589 | ||||||
chr11:897655
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.608+1685G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897655 | ||||||
chr11:897691
|
T | A | 17 | a0002c0002t0001g0005a0002c0002t0001g0035a0002c0002t0001g0193others(14): Show | 21 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.608+1649A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897691 | ||||||
chr11:897692
|
C | T | 17 | a0002c0002t0001g0005a0002c0002t0001g0035a0002c0002t0001g0193others(14): Show | 21 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.608+1648G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897692 | ||||||
chr11:897809
|
C | T | 1 | a0002c0002t0001g0284 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.608+1531G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897809 | ||||||
chr11:897825
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.608+1515T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897825 | ||||||
chr11:897981
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(45): Show | 59 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.608+1359G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897981 | ||||||
chr11:897995
|
G | C | 2 | a0001c0001t0001g0091a0002c0002t0024g0270 | 2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.608+1345C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897995 | ||||||
chr11:898074
|
A | C | 1 | a0002c0002t0001g0307 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.608+1266T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898074 | ||||||
chr11:898099
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.608+1241C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898099 | ||||||
chr11:898135
|
G | A | 9 | a0002c0002t0001g0212a0002c0002t0001g0219a0002c0002t0001g0220others(6): Show | 9 | NA18960.hp2 NA18965.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.608+1205C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898135 | ||||||
chr11:898155
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 252 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.608+1185A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898155 | ||||||
chr11:898162
|
A | G | 1 | a0002c0002t0024g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.608+1178T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898162 | ||||||
chr11:898344
|
T | C | 26 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(23): Show | 28 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.608+996A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898344 | ||||||
chr11:898352
|
G | T | 1 | a0002c0002t0001g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.608+988C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898352 | ||||||
chr11:898459
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.608+881T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898459 | ||||||
chr11:898463
|
T | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.608+877A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898463 | ||||||
chr11:898483
|
T | C | 1 | a0001c0001t0017g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.608+857A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898483 | ||||||
chr11:898518
|
G | A | 26 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(23): Show | 28 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.608+822C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898518 | ||||||
chr11:898643
|
C | T | 21 | a0001c0001t0001g0067a0001c0001t0001g0069a0002c0002t0001g0006others(18): Show | 23 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.608+697G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898643 | ||||||
chr11:898726
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.608+614G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898726 | ||||||
chr11:898743
|
T | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0146others(6): Show | 10 | HG00438.hp2 HG00597.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+597A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898743 | ||||||
chr11:898761
|
G | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0282 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.608+579C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898761 | ||||||
chr11:898892
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.608+448G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898892 | ||||||
chr11:898979
|
T | G | 1 | a0004c0004t0001g0318 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.608+361A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898979 | ||||||
chr11:899218
|
C | A | 1 | a0002c0002t0001g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.608+122G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 899218 | ||||||
chr11:899567
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.547-166C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899567 | ||||||
chr11:899580
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.547-179G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899580 | ||||||
chr11:899627
|
G | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(325): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.547-226C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899627 | ||||||
chr11:899814
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.546+190A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899814 | ||||||
chr11:899973
|
C | A | 1 | a0001c0001t0001g0314 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.546+31G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899973 | ||||||
chr11:900152
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.440-42T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900152 | ||||||
chr11:900183
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.440-73T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900183 | ||||||
chr11:900298
|
G | A | 2 | a0004c0004t0001g0038a0004c0004t0001g0318 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.440-188C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900298 | ||||||
chr11:900369
|
G | A | 26 | a0001c0001t0001g0097a0001c0001t0001g0162a0001c0001t0002g0019others(23): Show | 28 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.440-259C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900369 | ||||||
chr11:900421
|
T | C | 118 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(115): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.440-311A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900421 | ||||||
chr11:900485
|
T | C | 117 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(114): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.440-375A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900485 | ||||||
chr11:900690
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.439+246G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900690 | ||||||
chr11:900773
|
G | A | 1 | a0004c0004t0001g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.439+163C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900773 | ||||||
chr11:900809
|
G | A | 18 | a0002c0002t0001g0005a0002c0002t0001g0035a0002c0002t0001g0193others(15): Show | 22 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.439+127C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900809 | ||||||
chr11:900894
|
T | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.439+42A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900894 | ||||||
chr11:900929
|
C | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 261 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(258): Show |
splice_region_variant&intron_variant | LOW | c.439+7G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900929 | ||||||
chr11:901023
|
C | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0221 | 2 | HG02071.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.395-43G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901023 | ||||||
chr11:901177
|
C | CTTCT | 5 | a0002c0002t0001g0197a0002c0002t0001g0271a0002c0002t0001g0272others(2): Show | 5 | HG00642.hp1 HG02258.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-201_395-198dup others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901177 | ||||||
chr11:901337
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.395-357G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901337 | ||||||
chr11:901464
|
G | A | 2 | a0004c0004t0001g0038a0004c0004t0001g0318 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.395-484C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901464 | ||||||
chr11:901625
|
G | A | 4 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309others(1): Show | 4 | NA18979.hp1 NA18990.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+573C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901625 | ||||||
chr11:901690
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.394+508C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901690 | ||||||
chr11:901733
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 7 | HG02004.hp2 HG02683.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+465G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901733 | ||||||
chr11:901912
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.394+286C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901912 | ||||||
chr11:901935
|
CA | C | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.394+262delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901935 | ||||||
chr11:902036
|
TACAC | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 249 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.394+158_394+161del others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 902036 | ||||||
chr11:902045
|
A | G | 1 | a0002c0002t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.394+153T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 902045 | ||||||
chr11:902355
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0002g0019a0001c0001t0002g0098others(2): Show | 6 | HG03927.hp1 NA18967.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-25G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902355 | ||||||
chr11:902405
|
C | T | 23 | a0001c0001t0001g0067a0001c0001t0001g0069a0002c0002t0001g0006others(20): Show | 25 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.262-75G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902405 | ||||||
chr11:902645
|
G | A | 1 | a0002c0002t0001g0196 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.262-315C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902645 | ||||||
chr11:902668
|
AGGGTT | A | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.261+289_261+293del others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902668 | ||||||
chr11:902712
|
G | A | 3 | a0001c0001t0002g0163a0004c0004t0001g0038a0004c0004t0001g0318 | 3 | HG01167.hp1 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261+250C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902712 | ||||||
chr11:902742
|
C | G | 1 | a0003c0003t0002g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.261+220G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902742 | ||||||
chr11:902768
|
A | G | 2 | a0001c0001t0001g0018a0002c0002t0001g0079 | 3 | HG02572.hp2 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.261+194T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902768 | ||||||
chr11:902899
|
G | A | 2 | a0004c0004t0001g0038a0004c0004t0001g0318 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261+63C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902899 | ||||||
chr11:902939
|
G | A | 115 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0282others(112): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.261+23C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902939 | ||||||
chr11:903167
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.112-56G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903167 | ||||||
chr11:903214
|
T | A | 1 | a0002c0002t0001g0311 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.112-103A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903214 | ||||||
chr11:903216
|
T | C | 2 | a0002c0002t0001g0035a0002c0002t0001g0254 | 3 | HG00639.hp1 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.112-105A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903216 | ||||||
chr11:903260
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.112-149C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903260 | ||||||
chr11:903266
|
G | C | 3 | a0002c0002t0001g0034a0002c0002t0001g0312a0002c0002t0001g0313 | 4 | HG01346.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-155C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903266 | ||||||
chr11:903326
|
T | C | 35 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0028others(32): Show | 40 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-215A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903326 | ||||||
chr11:903332
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.112-221C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903332 | ||||||
chr11:903417
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.112-306C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903417 | ||||||
chr11:903470
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.112-359G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903470 | ||||||
chr11:903547
|
G | A | 1 | a0002c0002t0001g0315 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.112-436C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903547 | ||||||
chr11:903576
|
T | G | 1 | a0001c0001t0001g0029 | 2 | NA18948.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.112-465A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903576 | ||||||
chr11:903737
|
C | T | 1 | a0001c0001t0016g0080 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.112-626G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903737 | ||||||
chr11:903750
|
C | T | 1 | a0001c0001t0031g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.112-639G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903750 | ||||||
chr11:903838
|
C | T | 2 | a0002c0002t0001g0267a0002c0002t0001g0268 | 2 | NA18960.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.112-727G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903838 | ||||||
chr11:903847
|
G | GC | 8 | a0001c0001t0001g0185a0001c0001t0001g0206a0001c0001t0028g0184others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-737dupG | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903847 | ||||||
chr11:903897
|
G | A | 1 | a0002c0002t0001g0235 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.112-786C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903897 | ||||||
chr11:903977
|
C | A | 1 | a0001c0001t0017g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.111+729G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903977 | ||||||
chr11:904168
|
C | T | 3 | a0002c0002t0001g0222a0002c0002t0001g0242a0002c0002t0001g0243 | 3 | HG01167.hp2 HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.111+538G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904168 | ||||||
chr11:904258
|
G | A | 23 | a0001c0001t0001g0067a0001c0001t0001g0069a0002c0002t0001g0006others(20): Show | 25 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.111+448C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904258 | ||||||
chr11:904454
|
C | A | 25 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0019g0048others(22): Show | 27 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+252G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904454 | ||||||
chr11:904454
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.111+252G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904454 | ||||||
chr11:904563
|
C | T | 2 | a0002c0002t0001g0030a0002c0002t0001g0266 | 3 | NA18612.hp1 NA18965.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.111+143G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904563 | ||||||
chr11:904649
|
G | A | 2 | a0004c0004t0001g0038a0004c0004t0001g0318 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.111+57C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904649 | ||||||
chr11:904911
|
T | C | 144 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0069others(141): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.-43-52A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 904911 | ||||||
chr11:905331
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-43-472C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905331 | ||||||
chr11:905395
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-43-536G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905395 | ||||||
chr11:905441
|
G | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-582C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905441 | ||||||
chr11:905571
|
G | A | 1 | a0004c0004t0001g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43-712C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905571 | ||||||
chr11:905691
|
G | A | 1 | a0002c0002t0001g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-43-832C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905691 | ||||||
chr11:905719
|
C | T | 1 | a0002c0002t0005g0261 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-43-860G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905719 | ||||||
chr11:905740
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-43-881C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905740 | ||||||
chr11:906041
|
C | T | 3 | a0001c0001t0002g0043a0001c0001t0002g0322a0001c0001t0002g0323 | 3 | HG02486.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-43-1182G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906041 | ||||||
chr11:906081
|
GCCA | G | 3 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260 | 3 | HG01261.hp1 HG01358.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-43-1225_-43-1223d others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906081 | ||||||
chr11:906102
|
T | C | 1 | a0002c0002t0001g0320 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-43-1243A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906102 | ||||||
chr11:906173
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-43-1314T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906173 | ||||||
chr11:906210
|
C | T | 3 | a0001c0001t0001g0092a0002c0002t0001g0201a0002c0002t0027g0257 | 3 | HG00423.hp2 NA18952.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-43-1351G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906210 | ||||||
chr11:906241
|
C | CT | 13 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(10): Show | 13 | HG00741.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-43-1383dupA | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906241 | ||||||
chr11:906241
|
C | CTT | 8 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0039others(5): Show | 10 | HG02004.hp2 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-1384_-43-1383d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906241 | ||||||
chr11:906310
|
C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-43-1451G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906310 | ||||||
chr11:906380
|
A | G | 1 | a0004c0004t0001g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43-1521T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906380 | ||||||
chr11:906406
|
T | G | 1 | a0002c0002t0001g0321 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-43-1547A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906406 | ||||||
chr11:906513
|
G | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-1654C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906513 | ||||||
chr11:906535
|
C | T | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-1676G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906535 | ||||||
chr11:906636
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 5 | HG01175.hp2 HG01978.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-1777T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906636 | ||||||
chr11:906708
|
C | A | 119 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0052others(116): Show | 132 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-43-1849G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906708 | ||||||
chr11:906754
|
C | T | 5 | a0002c0002t0001g0223a0002c0002t0001g0224a0002c0002t0001g0233others(2): Show | 5 | NA18951.hp2 NA18966.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-1895G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906754 | ||||||
chr11:906767
|
G | A | 1 | a0002c0002t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-1908C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906767 | ||||||
chr11:906896
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-43-2037G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906896 | ||||||
chr11:906901
|
G | C | 1 | a0002c0002t0001g0037 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-43-2042C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906901 | ||||||
chr11:906984
|
C | T | 19 | a0001c0001t0001g0067a0001c0001t0001g0069a0002c0002t0001g0006others(16): Show | 21 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-43-2125G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906984 | ||||||
chr11:906985
|
G | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0002c0002t0001g0212 | 3 | NA18945.hp2 NA18947.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-43-2126C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906985 | ||||||
chr11:907086
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-2227T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907086 | ||||||
chr11:907206
|
G | T | 9 | a0001c0001t0001g0228a0002c0002t0001g0219a0002c0002t0001g0220others(6): Show | 9 | NA18952.hp1 NA18960.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-2347C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907206 | ||||||
chr11:907400
|
G | GA | 7 | a0002c0002t0001g0006a0002c0002t0001g0084a0002c0002t0001g0086others(4): Show | 9 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-2542dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907400 | ||||||
chr11:907457
|
G | C | 2 | a0001c0001t0002g0322a0001c0001t0002g0323 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-43-2598C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907457 | ||||||
chr11:907459
|
C | T | 4 | a0002c0002t0001g0223a0002c0002t0001g0224a0002c0002t0001g0225others(1): Show | 4 | HG02109.hp2 HG03471.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-2600G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907459 | ||||||
chr11:907479
|
TA | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 8 | HG01099.hp2 HG01167.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-2621delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907479 | ||||||
chr11:907510
|
A | G | 1 | a0002c0002t0001g0037 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-43-2651T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907510 | ||||||
chr11:907697
|
T | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 184 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.-43-2838A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907697 | ||||||
chr11:907699
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 184 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.-43-2840G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907699 | ||||||
chr11:907792
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-43-2933G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907792 | ||||||
chr11:907933
|
G | A | 1 | a0002c0002t0001g0324 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-44+2842C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907933 | ||||||
chr11:907936
|
C | T | 2 | a0002c0002t0001g0219a0002c0002t0001g0220 | 2 | NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-44+2839G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907936 | ||||||
chr11:908217
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-44+2558C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908217 | ||||||
chr11:908462
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-44+2313C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908462 | ||||||
chr11:908683
|
C | T | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+2092G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908683 | ||||||
chr11:908842
|
C | G | 1 | a0002c0002t0001g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-44+1933G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908842 | ||||||
chr11:908956
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44+1819G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908956 | ||||||
chr11:908992
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG00741.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-44+1783C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908992 | ||||||
chr11:909244
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-44+1531G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909244 | ||||||
chr11:909328
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-44+1447G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909328 | ||||||
chr11:909491
|
G | A | 1 | a0002c0002t0001g0035 | 2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-44+1284C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909491 | ||||||
chr11:909676
|
T | C | 1 | a0001c0001t0007g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-44+1099A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909676 | ||||||
chr11:909947
|
C | T | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+828G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909947 | ||||||
chr11:910058
|
C | CA | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0326others(3): Show | 6 | HG01175.hp2 NA18991.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+716dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910058 | ||||||
chr11:910097
|
A | G | 22 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0040others(19): Show | 24 | HG00741.hp1 HG01884.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.-44+678T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910097 | ||||||
chr11:910259
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 250 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.-44+516T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910259 | ||||||
chr11:910558
|
C | T | 1 | a0003c0003t0002g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44+217G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910558 |