geneid | 85395 |
---|---|
ensemblid | ENSG00000160256.14 |
hgncid | 15811 |
symbol | SLX9 |
name | SLX9 ribosome biogenesis factor |
refseq_nuc | NM_058190.4 |
refseq_prot | NP_478070.1 |
ensembl_nuc | ENST00000291634.11 |
ensembl_prot | ENSP00000291634.6 |
mane_status | MANE Select |
chr | chr21 |
start | 44940029 |
end | 44976973 |
strand | + |
ver | v1.2 |
region | chr21:44940029-44976973 |
region5000 | chr21:44935029-44981973 |
regionname0 | SLX9_chr21_44940029_44976973 |
regionname5000 | SLX9_chr21_44935029_44981973 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 230 | 273 | 37 | 51 | 128 | 17 | 38 | 85 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0002 | 0/0 | 230 | 26 | 3 | 1 | 20 | 1 | 1 | 15 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0003 | 0/0 | 230 | 20 | 13 | 6 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0004 | 0/0 | 230 | 13 | 2 | 8 | 2 | 0 | 1 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0005 | 0/0 | 215 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0006 | 0/0 | 230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 693 | 271 | 37 | 49 | 128 | 17 | 38 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
c0002 | 0/0 | 693 | 26 | 3 | 1 | 20 | 1 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
c0003 | 0/0 | 693 | 20 | 13 | 6 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
c0004 | 0/0 | 693 | 13 | 2 | 8 | 2 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
c0005 | 0/0 | 693 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
c0006 | 0/0 | 693 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
c0007 | 0/0 | 648 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 200 | 334 | 56 | 66 | 150 | 18 | 42 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0003 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0005 | 0/0 | 7 | 0 | 4 | 2 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0006 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0014 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 693 | 271 | 37 | 49 | 128 | 17 | 38 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0001c0005 | 0/0 | 693 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0002c0002 | 0/0 | 693 | 26 | 3 | 1 | 20 | 1 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0003c0003 | 0/0 | 693 | 20 | 13 | 6 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0004c0004 | 0/0 | 693 | 13 | 2 | 8 | 2 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0005c0007 | 0/0 | 648 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0006c0006 | 0/0 | 693 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 892 | 271 | 37 | 49 | 128 | 17 | 38 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0001c0005t0001 | 0/0 | 892 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0002c0002t0001 | 0/0 | 892 | 26 | 3 | 1 | 20 | 1 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0003c0003t0001 | 0/0 | 892 | 20 | 13 | 6 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0004c0004t0001 | 0/0 | 892 | 13 | 2 | 8 | 2 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0005c0007t0001 | 0/0 | 847 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
a0006c0006t0001 | 0/0 | 892 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | copy fasta | chr21 | 44935029 | 44981973 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 4 | 2 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0001c0005t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0003c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0004c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0005c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
a0006c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0206 | EUR | FIN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG00738 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01069 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01168 | hp2 | a0004 | c0004 | t0001 | g0017 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0217 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0181 | AMR | PUR | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01255 | hp1 | a0004 | c0004 | t0001 | g0223 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01361 | hp1 | a0004 | c0004 | t0001 | g0225 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01433 | hp1 | a0004 | c0004 | t0001 | g0017 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01496 | hp1 | a0004 | c0004 | t0001 | g0224 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0142 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01891 | hp1 | a0003 | c0003 | t0001 | g0121 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01952 | hp1 | a0004 | c0004 | t0001 | g0222 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0218 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02004 | hp1 | a0004 | c0004 | t0001 | g0042 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02257 | hp1 | a0003 | c0003 | t0001 | g0047 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02300 | hp2 | a0004 | c0004 | t0001 | g0042 | AMR | PEL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0131 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0053 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0132 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03516 | hp1 | a0003 | c0003 | t0001 | g0130 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03579 | hp1 | a0006 | c0006 | t0001 | g0137 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04115 | hp2 | a0005 | c0007 | t0001 | g0101 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04199 | hp2 | a0004 | c0004 | t0001 | g0017 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18981 | hp2 | a0004 | c0004 | t0001 | g0227 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | LWK | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19083 | hp1 | a0004 | c0004 | t0001 | g0219 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19240 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | YRI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0216 | SAS | GIH | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01123 | hp1 | a0001 | c0005 | t0001 | g0096 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0135 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0052 | AFR | ACB | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20300 | hp1 | a0004 | c0004 | t0001 | g0220 | AFR | USA | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
NA21309 | hp2 | a0004 | c0004 | t0001 | g0221 | AFR | LWK | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0059 | REF | REF | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0195 | REF | REF | SLX9_chr21_44935029_44981973 | SLX9 | chr21 | 44935029 | 44981973 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:44940161
|
C | T | 1 | a0004 | 13 | HG01168.hp2 HG01255.hp1 HG01361.hp1 others(10): Show |
missense_variant | MODERATE | c.104C>T | p.Pro35Leu | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/6 | 133/892 | 104/693 | 35/230 | chr21 | 44940161 | ||
chr21:44943783
|
GTCAGGAG others(38): Show |
G | 1 | a0005 | 1 | HG04115.hp2 | splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.254_283+15delGTGCA others(40): Show |
p.Ala86_Gly95del | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/6 | 283/892 | 254/693 | 85/230 | INFO_REALIGN_3_PRIME | chr21 | 44943783 | |
chr21:44967163
|
G | T | 2 | a0002a0004 | 39 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(36): Show |
missense_variant | MODERATE | c.482G>T | p.Ser161Ile | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/6 | 511/892 | 482/693 | 161/230 | chr21 | 44967163 | ||
chr21:44976690
|
A | G | 1 | a0006 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.580A>G | p.Arg194Gly | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 6/6 | 609/892 | 580/693 | 194/230 | chr21 | 44976690 | ||
chr21:44976744
|
G | C | 3 | a0002a0003a0004 | 59 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
missense_variant | MODERATE | c.634G>C | p.Val212Leu | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 6/6 | 663/892 | 634/693 | 212/230 | chr21 | 44976744 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:44943692
|
G | A | 1 | a0001c0005 | 2 | HG00738.hp2 HG01123.hp1 |
synonymous_variant | LOW | c.138G>A | p.Ala46Ala | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/6 | 167/892 | 138/693 | 46/230 | chr21 | 44943692 |
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 |
---|
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:44940292
|
G | T | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+106G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940292 | ||||||
chr21:44940338
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.129+152C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940338 | ||||||
chr21:44940382
|
G | T | 33 | a0001c0001t0001g0226a0002c0002t0001g0002a0002c0002t0001g0204others(30): Show | 46 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.129+196G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940382 | ||||||
chr21:44940567
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.129+381A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940567 | ||||||
chr21:44940571
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.129+385G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940571 | ||||||
chr21:44940624
|
T | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0030others(97): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.129+438T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940624 | ||||||
chr21:44940652
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0030others(96): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.129+466G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940652 | ||||||
chr21:44940672
|
A | AT | 5 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0049others(2): Show | 11 | HG00438.hp1 HG01167.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+501dupT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940672 | |||||
chr21:44940672
|
A | ATT | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.129+500_129+501dup others(2): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940672 | |||||
chr21:44940672
|
A | ATTT | 12 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(9): Show | 13 | HG00544.hp2 HG01358.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+499_129+501dup others(3): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940672 | |||||
chr21:44940672
|
A | ATTTT | 6 | a0001c0001t0001g0134a0003c0003t0001g0130a0003c0003t0001g0131others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+498_129+501dup others(4): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940672 | |||||
chr21:44940672
|
ATT | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(50): Show | 71 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.129+500_129+501del others(2): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940672 | |||||
chr21:44940672
|
ATTT | A | 46 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0044others(43): Show | 60 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.129+499_129+501del others(3): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940672 | |||||
chr21:44940698
|
T | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0030others(96): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.129+512T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940698 | ||||||
chr21:44940734
|
C | CTT | 97 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0030others(94): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.129+549_129+550ins others(2): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44940734 | |||||
chr21:44940800
|
C | T | 36 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(33): Show | 49 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.129+614C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940800 | ||||||
chr21:44940842
|
C | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0030others(96): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.129+656C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44940842 | ||||||
chr21:44941008
|
G | GCTTTTGA others(2): Show |
99 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0030others(96): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.129+827_129+835dup others(9): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44941008 | |||||
chr21:44941017
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02027.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.129+831C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941017 | ||||||
chr21:44941101
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.129+915A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941101 | ||||||
chr21:44941103
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.129+917A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941103 | ||||||
chr21:44941151
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.129+965C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941151 | ||||||
chr21:44941197
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.129+1011A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941197 | ||||||
chr21:44941271
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.129+1085A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941271 | ||||||
chr21:44941358
|
CTGCTTGA | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(8): Show | 13 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.129+1174_129+1180d others(9): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr21 | 44941358 | |||||
chr21:44941380
|
G | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(2): Show | 7 | HG01167.hp1 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1194G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941380 | ||||||
chr21:44941417
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.129+1231C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941417 | ||||||
chr21:44941509
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.129+1323A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941509 | ||||||
chr21:44941516
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.129+1330T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941516 | ||||||
chr21:44941707
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.129+1521G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941707 | ||||||
chr21:44941720
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.129+1534C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941720 | ||||||
chr21:44941847
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129+1661C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941847 | ||||||
chr21:44941890
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.129+1704G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941890 | ||||||
chr21:44941906
|
C | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0134a0001c0001t0001g0138others(14): Show | 18 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.129+1720C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941906 | ||||||
chr21:44941910
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.129+1724C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44941910 | ||||||
chr21:44942068
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130-1616A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942068 | ||||||
chr21:44942138
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01978.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.130-1546A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942138 | ||||||
chr21:44942181
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.130-1503G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942181 | ||||||
chr21:44942244
|
C | T | 33 | a0001c0001t0001g0226a0002c0002t0001g0002a0002c0002t0001g0204others(30): Show | 46 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.130-1440C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942244 | ||||||
chr21:44942293
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 82 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.130-1391C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942293 | ||||||
chr21:44942357
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130-1327T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942357 | ||||||
chr21:44942375
|
T | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(94): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.130-1309T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942375 | ||||||
chr21:44942456
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.130-1228G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942456 | ||||||
chr21:44942468
|
A | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(94): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.130-1216A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942468 | ||||||
chr21:44942568
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.130-1116G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942568 | ||||||
chr21:44942622
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.130-1062A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942622 | ||||||
chr21:44942635
|
A | G | 33 | a0001c0001t0001g0226a0002c0002t0001g0002a0002c0002t0001g0204others(30): Show | 46 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.130-1049A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942635 | ||||||
chr21:44942749
|
C | T | 2 | a0002c0002t0001g0230a0002c0002t0001g0232 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130-935C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942749 | ||||||
chr21:44942777
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.130-907A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942777 | ||||||
chr21:44942783
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130-901A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942783 | ||||||
chr21:44942878
|
A | G | 2 | a0001c0001t0001g0200a0002c0002t0001g0231 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.130-806A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942878 | ||||||
chr21:44942931
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130-753A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44942931 | ||||||
chr21:44943132
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-552G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943132 | ||||||
chr21:44943380
|
T | C | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG00408.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.130-304T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943380 | ||||||
chr21:44943443
|
C | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-241C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943443 | ||||||
chr21:44943484
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.130-200T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943484 | ||||||
chr21:44943519
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(93): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.130-165T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943519 | ||||||
chr21:44943541
|
G | T | 1 | a0001c0001t0001g0054 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.130-143G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943541 | ||||||
chr21:44943559
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.130-125C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 1/5 | chr21 | 44943559 | ||||||
chr21:44944037
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(93): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.283+200T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944037 | ||||||
chr21:44944040
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+203G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944040 | ||||||
chr21:44944308
|
C | T | 33 | a0001c0001t0001g0226a0002c0002t0001g0002a0002c0002t0001g0204others(30): Show | 46 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.283+471C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944308 | ||||||
chr21:44944321
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+484G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944321 | ||||||
chr21:44944379
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.283+542G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944379 | ||||||
chr21:44944430
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+593C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944430 | ||||||
chr21:44944434
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.283+597C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944434 | ||||||
chr21:44944474
|
TC | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+640delC | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44944474 | |||||
chr21:44944755
|
C | T | 1 | a0002c0002t0001g0228 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.283+918C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944755 | ||||||
chr21:44944925
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+1088T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944925 | ||||||
chr21:44944951
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+1114C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44944951 | ||||||
chr21:44945034
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+1197C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945034 | ||||||
chr21:44945037
|
G | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0233 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.283+1200G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945037 | ||||||
chr21:44945056
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+1219A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945056 | ||||||
chr21:44945063
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+1226G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945063 | ||||||
chr21:44945166
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+1329A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945166 | ||||||
chr21:44945271
|
C | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+1434C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945271 | ||||||
chr21:44945326
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+1489C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945326 | ||||||
chr21:44945574
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+1737G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945574 | ||||||
chr21:44945628
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.283+1791G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945628 | ||||||
chr21:44945686
|
A | C | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+1849A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945686 | ||||||
chr21:44945709
|
TTTTG | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(2): Show | 7 | HG01167.hp1 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+1889_283+1892d others(6): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44945709 | |||||
chr21:44945829
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+1992G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945829 | ||||||
chr21:44945842
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.283+2005C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945842 | ||||||
chr21:44945897
|
G | T | 1 | a0002c0002t0001g0228 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.283+2060G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945897 | ||||||
chr21:44945943
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(17): Show | 31 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.283+2106C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945943 | ||||||
chr21:44945955
|
G | C | 1 | a0006c0006t0001g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+2118G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44945955 | ||||||
chr21:44946085
|
G | GGAGAGGG others(58): Show |
1 | a0004c0004t0001g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.283+2249_283+2313d others(67): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44946085 | |||||
chr21:44946238
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+2401T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44946238 | ||||||
chr21:44946309
|
T | TGTAGCGT others(89): Show |
4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+2543_283+2544i others(98): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44946309 | |||||
chr21:44946314
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+2477C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44946314 | ||||||
chr21:44946451
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.283+2614G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44946451 | ||||||
chr21:44946622
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+2785C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44946622 | ||||||
chr21:44946632
|
T | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(58): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.283+2795T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44946632 | ||||||
chr21:44947038
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283+3201C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947038 | ||||||
chr21:44947039
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.283+3202G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947039 | ||||||
chr21:44947147
|
T | C | 15 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(12): Show | 23 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.283+3310T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947147 | ||||||
chr21:44947205
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0125 | 2 | HG00639.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.283+3368G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947205 | ||||||
chr21:44947341
|
G | C | 31 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(28): Show | 44 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.283+3504G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947341 | ||||||
chr21:44947438
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+3601C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947438 | ||||||
chr21:44947442
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 9 | HG00673.hp1 HG01358.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+3605G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947442 | ||||||
chr21:44947480
|
A | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(4): Show | 8 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+3643A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947480 | ||||||
chr21:44947533
|
G | GTGGCATC others(27): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0058others(1): Show | 5 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+3746_283+3779d others(36): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44947533 | |||||
chr21:44947533
|
GTGGCATC others(27): Show |
G | 8 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0143others(5): Show | 10 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+3746_283+3779d others(36): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44947533 | |||||
chr21:44947835
|
C | A | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.283+3998C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947835 | ||||||
chr21:44947868
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+4031C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44947868 | ||||||
chr21:44948001
|
C | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+4164C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948001 | ||||||
chr21:44948026
|
TG | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4190delG | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948026 | ||||||
chr21:44948084
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.283+4247T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948084 | ||||||
chr21:44948126
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.283+4289A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948126 | ||||||
chr21:44948230
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+4393G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948230 | ||||||
chr21:44948283
|
C | G | 32 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(29): Show | 45 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.283+4446C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948283 | ||||||
chr21:44948298
|
C | A | 37 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(34): Show | 50 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.283+4461C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948298 | ||||||
chr21:44948303
|
GGTCCGGG others(23): Show |
G | 1 | a0002c0002t0001g0206 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283+4513_283+4542d others(32): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44948303 | |||||
chr21:44948308
|
G | A | 1 | a0003c0003t0001g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.283+4471G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948308 | ||||||
chr21:44948319
|
C | T | 1 | a0001c0001t0001g0039 | 2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.283+4482C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948319 | ||||||
chr21:44948333
|
C | CG | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+4497dupG | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44948333 | |||||
chr21:44948337
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0079others(3): Show | 11 | HG00621.hp1 HG01358.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+4500C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948337 | ||||||
chr21:44948362
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02145.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283+4525G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948362 | ||||||
chr21:44948410
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+4573C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948410 | ||||||
chr21:44948543
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+4706A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948543 | ||||||
chr21:44948549
|
A | G | 37 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(34): Show | 50 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.283+4712A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948549 | ||||||
chr21:44948665
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+4828C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948665 | ||||||
chr21:44948677
|
G | A | 13 | a0001c0001t0001g0048a0001c0001t0001g0134a0003c0003t0001g0029others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+4840G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948677 | ||||||
chr21:44948694
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.283+4857C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948694 | ||||||
chr21:44948705
|
G | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4868G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948705 | ||||||
chr21:44948802
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+4965T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948802 | ||||||
chr21:44948886
|
G | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0216a0003c0003t0001g0217others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+5049G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948886 | ||||||
chr21:44948940
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.283+5103A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44948940 | ||||||
chr21:44949125
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 15 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+5288G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949125 | ||||||
chr21:44949179
|
G | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(5): Show | 10 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+5342G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949179 | ||||||
chr21:44949271
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+5434C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949271 | ||||||
chr21:44949316
|
T | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+5479T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949316 | ||||||
chr21:44949339
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(42): Show | 62 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+5502G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949339 | ||||||
chr21:44949372
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.283+5535C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949372 | ||||||
chr21:44949377
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+5540G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949377 | ||||||
chr21:44949391
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+5554G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949391 | ||||||
chr21:44949397
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+5560G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949397 | ||||||
chr21:44949398
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+5561C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949398 | ||||||
chr21:44949538
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+5701C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949538 | ||||||
chr21:44949565
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283+5728A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949565 | ||||||
chr21:44949573
|
A | C | 13 | a0001c0001t0001g0048a0001c0001t0001g0134a0003c0003t0001g0029others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+5736A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949573 | ||||||
chr21:44949616
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0078 | 4 | HG02683.hp2 HG03927.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5779G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949616 | ||||||
chr21:44949648
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(5): Show | 10 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+5811C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949648 | ||||||
chr21:44949693
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG02027.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.283+5856G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949693 | ||||||
chr21:44949860
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.283+6023C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949860 | ||||||
chr21:44949870
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+6033A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949870 | ||||||
chr21:44949999
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.283+6162A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44949999 | ||||||
chr21:44950032
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+6195G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950032 | ||||||
chr21:44950100
|
AT | A | 41 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0044others(38): Show | 55 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.283+6277delT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44950100 | |||||
chr21:44950115
|
A | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 6 | HG04184.hp1 NA18959.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6278A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950115 | ||||||
chr21:44950117
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.283+6280G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950117 | ||||||
chr21:44950134
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.283+6297A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950134 | ||||||
chr21:44950236
|
CA | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(9): Show | 15 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+6411delA | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44950236 | |||||
chr21:44950297
|
AG | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.283+6462delG | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44950297 | |||||
chr21:44950363
|
G | A | 17 | a0001c0001t0001g0048a0001c0001t0001g0134a0001c0001t0001g0138others(14): Show | 18 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.283+6526G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950363 | ||||||
chr21:44950507
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.283+6670A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950507 | ||||||
chr21:44950520
|
G | A | 1 | a0003c0003t0001g0016 | 3 | HG01069.hp1 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.283+6683G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950520 | ||||||
chr21:44950529
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.283+6692G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950529 | ||||||
chr21:44950584
|
A | G | 1 | a0001c0001t0001g0024 | 2 | NA18984.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.283+6747A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950584 | ||||||
chr21:44950597
|
G | T | 1 | a0001c0001t0001g0041 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.283+6760G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950597 | ||||||
chr21:44950627
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.283+6790G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950627 | ||||||
chr21:44950645
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.283+6808G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950645 | ||||||
chr21:44950676
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283+6839T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950676 | ||||||
chr21:44950821
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+6984G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950821 | ||||||
chr21:44950856
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+7019G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950856 | ||||||
chr21:44950862
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+7025G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950862 | ||||||
chr21:44950882
|
CTGTGGGT others(986): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+7360_284-7911d others(2): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44950882 | |||||
chr21:44950934
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.283+7097G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950934 | ||||||
chr21:44950993
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(28): Show | 44 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.283+7156C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44950993 | ||||||
chr21:44951044
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.283+7207C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951044 | ||||||
chr21:44951050
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.283+7213C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951050 | ||||||
chr21:44951062
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.283+7225G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951062 | ||||||
chr21:44951065
|
G | A | 32 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(29): Show | 45 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.283+7228G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951065 | ||||||
chr21:44951134
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283+7297T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951134 | ||||||
chr21:44951163
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 9 | HG00673.hp1 HG01358.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+7326G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951163 | ||||||
chr21:44951188
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283+7351A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951188 | ||||||
chr21:44951194
|
G | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+7357G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951194 | ||||||
chr21:44951212
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+7375C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951212 | ||||||
chr21:44951275
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.283+7438C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951275 | ||||||
chr21:44951282
|
A | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+7445A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951282 | ||||||
chr21:44951290
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+7453C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951290 | ||||||
chr21:44951431
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+7594C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951431 | ||||||
chr21:44951602
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(5): Show | 11 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+7765G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951602 | ||||||
chr21:44951666
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.283+7829C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951666 | ||||||
chr21:44951754
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.283+7917G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951754 | ||||||
chr21:44951789
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+7952G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951789 | ||||||
chr21:44951873
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0165 | 3 | NA18941.hp2 NA19004.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.283+8036G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951873 | ||||||
chr21:44951878
|
TGGGTTTA others(310): Show |
T | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+8044_284-7903d others(2): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44951878 | |||||
chr21:44951955
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.283+8118G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44951955 | ||||||
chr21:44952254
|
T | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-7846T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44952254 | ||||||
chr21:44952299
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-7801C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44952299 | ||||||
chr21:44952550
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.284-7550C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44952550 | ||||||
chr21:44952588
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(28): Show | 44 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.284-7512C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44952588 | ||||||
chr21:44952640
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-7460T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44952640 | ||||||
chr21:44952802
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG00323.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.284-7298C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44952802 | ||||||
chr21:44953232
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6868C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44953232 | ||||||
chr21:44953256
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0058 | 3 | HG00140.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.284-6844G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44953256 | ||||||
chr21:44953435
|
G | GGCACCAT others(44): Show |
3 | a0002c0002t0001g0207a0002c0002t0001g0208a0002c0002t0001g0209 | 3 | NA18964.hp2 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.284-6654_284-6653i others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953435 | |||||
chr21:44953435
|
G | GGCACCAT others(44): Show |
1 | a0003c0003t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.284-6648_284-6647i others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953435 | |||||
chr21:44953435
|
G | GGCACCAT others(44): Show |
16 | a0001c0001t0001g0048a0001c0001t0001g0134a0001c0001t0001g0138others(13): Show | 17 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-6648_284-6647i others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953435 | |||||
chr21:44953435
|
G | GGCACCAT others(44): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-6632_284-6631i others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953435 | |||||
chr21:44953435
|
G | GGCACCAT others(44): Show |
75 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(72): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.284-6637_284-6587d others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953435 | |||||
chr21:44953435
|
G | GGCACCAT others(44): Show |
1 | a0001c0001t0001g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-6655_284-6654i others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953435 | |||||
chr21:44953449
|
C | CGGTGGGG others(46): Show |
1 | a0004c0004t0001g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.284-6641_284-6640i others(55): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953449 | |||||
chr21:44953463
|
GTCCGGGC others(44): Show |
G | 1 | a0001c0001t0001g0110 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.284-6561_284-6511d others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953463 | |||||
chr21:44953495
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-6605C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44953495 | ||||||
chr21:44953498
|
G | GGCGGTGG others(44): Show |
1 | a0001c0001t0001g0136 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.284-6587_284-6586i others(53): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44953498 | |||||
chr21:44953514
|
A | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0038others(13): Show | 20 | HG01099.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.284-6586A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44953514 | ||||||
chr21:44953565
|
A | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-6535A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44953565 | ||||||
chr21:44953789
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-6311C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44953789 | ||||||
chr21:44954071
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(7): Show | 13 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-6029A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954071 | ||||||
chr21:44954119
|
G | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(5): Show | 10 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-5981G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954119 | ||||||
chr21:44954123
|
T | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-5977T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954123 | ||||||
chr21:44954144
|
T | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-5956T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954144 | ||||||
chr21:44954162
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-5938C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954162 | ||||||
chr21:44954209
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-5891G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954209 | ||||||
chr21:44954314
|
T | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(84): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.284-5786T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954314 | ||||||
chr21:44954470
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18747.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.284-5630G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954470 | ||||||
chr21:44954573
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-5527C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954573 | ||||||
chr21:44954683
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-5417T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954683 | ||||||
chr21:44954697
|
C | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0134a0001c0001t0001g0138others(14): Show | 18 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-5403C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954697 | ||||||
chr21:44954721
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.284-5379T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954721 | ||||||
chr21:44954868
|
A | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-5232A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954868 | ||||||
chr21:44954942
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.284-5158G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44954942 | ||||||
chr21:44955008
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-5092G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955008 | ||||||
chr21:44955079
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-5021G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955079 | ||||||
chr21:44955082
|
G | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(41): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-5018G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955082 | ||||||
chr21:44955136
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.284-4964A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955136 | ||||||
chr21:44955162
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0057 | 8 | HG00558.hp2 HG02132.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-4938C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955162 | ||||||
chr21:44955207
|
C | CA | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.284-4878dupA | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44955207 | |||||
chr21:44955248
|
G | C | 1 | a0002c0002t0001g0210 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.284-4852G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955248 | ||||||
chr21:44955254
|
CAG | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0143others(6): Show | 11 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-4845_284-4844d others(4): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955254 | ||||||
chr21:44955266
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-4834C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955266 | ||||||
chr21:44955439
|
A | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(42): Show | 62 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.284-4661A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955439 | ||||||
chr21:44955672
|
G | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0092others(2): Show | 6 | HG02015.hp2 HG02027.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-4428G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955672 | ||||||
chr21:44955684
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.284-4416C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955684 | ||||||
chr21:44955735
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-4365C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955735 | ||||||
chr21:44955768
|
A | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(6): Show | 12 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-4332A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955768 | ||||||
chr21:44955803
|
G | C | 36 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(33): Show | 49 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.284-4297G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955803 | ||||||
chr21:44955827
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.284-4273G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955827 | ||||||
chr21:44955835
|
AT | A | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | NA18747.hp1 NA18955.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-4262delT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr21 | 44955835 | |||||
chr21:44955889
|
G | A | 36 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(33): Show | 49 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.284-4211G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955889 | ||||||
chr21:44955929
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 14 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(11): Show |
intron_variant | MODIFIER | c.284-4171C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955929 | ||||||
chr21:44955968
|
TG | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(17): Show | 31 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.284-4131delG | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955968 | ||||||
chr21:44955994
|
T | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-4106T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955994 | ||||||
chr21:44955997
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-4103C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44955997 | ||||||
chr21:44956001
|
T | C | 20 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(17): Show | 24 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.284-4099T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956001 | ||||||
chr21:44956149
|
G | A | 1 | a0001c0001t0001g0027 | 2 | NA18940.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.284-3951G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956149 | ||||||
chr21:44956500
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-3600C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956500 | ||||||
chr21:44956595
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-3505G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956595 | ||||||
chr21:44956613
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.284-3487A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956613 | ||||||
chr21:44956691
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-3409C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956691 | ||||||
chr21:44956756
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(41): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-3344G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956756 | ||||||
chr21:44956780
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-3320C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956780 | ||||||
chr21:44956827
|
C | T | 1 | a0001c0001t0001g0038 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.284-3273C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956827 | ||||||
chr21:44956967
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.284-3133A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44956967 | ||||||
chr21:44957082
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-3018C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957082 | ||||||
chr21:44957086
|
C | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0134a0001c0001t0001g0138others(14): Show | 18 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-3014C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957086 | ||||||
chr21:44957149
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(41): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-2951G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957149 | ||||||
chr21:44957205
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.284-2895G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957205 | ||||||
chr21:44957342
|
C | G | 2 | a0003c0003t0001g0217a0003c0003t0001g0218 | 2 | HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.284-2758C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957342 | ||||||
chr21:44957358
|
G | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-2742G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957358 | ||||||
chr21:44957359
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-2741C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957359 | ||||||
chr21:44957370
|
C | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0134a0003c0003t0001g0029others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.284-2730C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957370 | ||||||
chr21:44957439
|
C | T | 1 | a0004c0004t0001g0224 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.284-2661C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957439 | ||||||
chr21:44957517
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.284-2583G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957517 | ||||||
chr21:44957569
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(4): Show | 10 | HG01167.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-2531G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957569 | ||||||
chr21:44957691
|
C | T | 1 | a0003c0003t0001g0133 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.284-2409C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957691 | ||||||
chr21:44957838
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.284-2262T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44957838 | ||||||
chr21:44958030
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.284-2070C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958030 | ||||||
chr21:44958282
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0043others(7): Show | 12 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-1818A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958282 | ||||||
chr21:44958384
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284-1716G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958384 | ||||||
chr21:44958477
|
A | G | 14 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0043others(11): Show | 16 | HG01243.hp2 HG02258.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-1623A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958477 | ||||||
chr21:44958524
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(41): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-1576G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958524 | ||||||
chr21:44958532
|
G | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.284-1568G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958532 | ||||||
chr21:44958578
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-1522C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958578 | ||||||
chr21:44958579
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.284-1521G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958579 | ||||||
chr21:44958649
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0165 | 3 | NA18941.hp2 NA19004.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.284-1451G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958649 | ||||||
chr21:44958718
|
G | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0216a0003c0003t0001g0217others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-1382G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958718 | ||||||
chr21:44958772
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.284-1328C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958772 | ||||||
chr21:44958854
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.284-1246A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958854 | ||||||
chr21:44958893
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-1207C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958893 | ||||||
chr21:44958896
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.284-1204G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958896 | ||||||
chr21:44958995
|
G | A | 1 | a0001c0001t0001g0059 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284-1105G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44958995 | ||||||
chr21:44959026
|
G | A | 10 | a0004c0004t0001g0017a0004c0004t0001g0042a0004c0004t0001g0219others(7): Show | 13 | HG01168.hp2 HG01255.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-1074G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959026 | ||||||
chr21:44959048
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0075 | 3 | NA18959.hp1 NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.284-1052A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959048 | ||||||
chr21:44959057
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-1043A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959057 | ||||||
chr21:44959072
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-1028G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959072 | ||||||
chr21:44959101
|
A | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-999A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959101 | ||||||
chr21:44959109
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-991G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959109 | ||||||
chr21:44959277
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0180a0001c0001t0001g0182others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-823C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959277 | ||||||
chr21:44959308
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-792G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959308 | ||||||
chr21:44959323
|
C | T | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG01978.hp1 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-777C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959323 | ||||||
chr21:44959474
|
C | T | 31 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(28): Show | 44 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.284-626C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959474 | ||||||
chr21:44959511
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-589A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959511 | ||||||
chr21:44959521
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.284-579G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959521 | ||||||
chr21:44959621
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.284-479C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959621 | ||||||
chr21:44959630
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-470T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959630 | ||||||
chr21:44959658
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.284-442C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959658 | ||||||
chr21:44959686
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-414A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959686 | ||||||
chr21:44959721
|
T | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(90): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.284-379T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959721 | ||||||
chr21:44959733
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(32): Show | 63 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.284-367C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959733 | ||||||
chr21:44959761
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.284-339G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959761 | ||||||
chr21:44959777
|
A | G | 1 | a0003c0003t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.284-323A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959777 | ||||||
chr21:44959846
|
G | A | 2 | a0002c0002t0001g0211a0002c0002t0001g0229 | 2 | HG02040.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.284-254G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44959846 | ||||||
chr21:44960052
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-48A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 2/5 | chr21 | 44960052 | ||||||
chr21:44960223
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.352+55G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960223 | ||||||
chr21:44960425
|
G | A | 2 | a0002c0002t0001g0212a0002c0002t0001g0231 | 2 | HG01891.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.352+257G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960425 | ||||||
chr21:44960433
|
A | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185 | 4 | HG02630.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+265A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960433 | ||||||
chr21:44960565
|
G | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+397G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960565 | ||||||
chr21:44960638
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.352+470A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960638 | ||||||
chr21:44960641
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+473G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960641 | ||||||
chr21:44960736
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+568C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960736 | ||||||
chr21:44960759
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.352+591G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960759 | ||||||
chr21:44960820
|
T | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0116 | 6 | NA18969.hp1 NA19007.hp1 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+652T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960820 | ||||||
chr21:44960960
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+792T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44960960 | ||||||
chr21:44961128
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.352+960C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961128 | ||||||
chr21:44961147
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.352+979C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961147 | ||||||
chr21:44961153
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+985A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961153 | ||||||
chr21:44961291
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.352+1123G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961291 | ||||||
chr21:44961450
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.352+1282A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961450 | ||||||
chr21:44961604
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01346.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.352+1436C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961604 | ||||||
chr21:44961649
|
T | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(41): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.352+1481T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961649 | ||||||
chr21:44961671
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+1503C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961671 | ||||||
chr21:44961687
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352+1519C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961687 | ||||||
chr21:44961690
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(84): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.352+1522C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961690 | ||||||
chr21:44961702
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.352+1534T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961702 | ||||||
chr21:44961809
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0092others(2): Show | 6 | HG02015.hp2 HG02027.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+1641G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961809 | ||||||
chr21:44961985
|
G | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+1817G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44961985 | ||||||
chr21:44962000
|
C | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(2): Show | 7 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+1832C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962000 | ||||||
chr21:44962084
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.352+1916C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962084 | ||||||
chr21:44962191
|
A | G | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.352+2023A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962191 | ||||||
chr21:44962297
|
C | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0134a0003c0003t0001g0029others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.352+2129C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962297 | ||||||
chr21:44962307
|
G | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0134others(16): Show | 21 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.352+2139G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962307 | ||||||
chr21:44962724
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.352+2556G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962724 | ||||||
chr21:44962820
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.352+2652A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962820 | ||||||
chr21:44962824
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.352+2656A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962824 | ||||||
chr21:44962837
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.352+2669T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44962837 | ||||||
chr21:44963015
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.352+2847C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963015 | ||||||
chr21:44963092
|
C | CT | 9 | a0001c0001t0001g0014a0001c0001t0001g0102a0001c0001t0001g0103others(6): Show | 11 | HG01069.hp2 HG01346.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.352+2939dupT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr21 | 44963092 | |||||
chr21:44963148
|
G | C | 31 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(28): Show | 44 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.352+2980G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963148 | ||||||
chr21:44963214
|
G | A | 1 | a0004c0004t0001g0225 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.352+3046G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963214 | ||||||
chr21:44963277
|
G | A | 1 | a0003c0003t0001g0216 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.352+3109G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963277 | ||||||
chr21:44963293
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.352+3125G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963293 | ||||||
chr21:44963331
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0136a0001c0001t0001g0164others(3): Show | 13 | HG00423.hp2 HG00621.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.352+3163G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963331 | ||||||
chr21:44963354
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0031others(42): Show | 62 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.352+3186C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963354 | ||||||
chr21:44963375
|
C | CT | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.352+3222dupT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr21 | 44963375 | |||||
chr21:44963375
|
CT | C | 32 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(29): Show | 45 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.352+3222delT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr21 | 44963375 | |||||
chr21:44963390
|
T | TA | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+3225dupA | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr21 | 44963390 | |||||
chr21:44963391
|
A | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0041others(4): Show | 10 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.352+3223A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963391 | ||||||
chr21:44963484
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.352+3316T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963484 | ||||||
chr21:44963539
|
G | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.352+3371G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963539 | ||||||
chr21:44963759
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.353-3275T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963759 | ||||||
chr21:44963764
|
C | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(3): Show | 7 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.353-3270C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44963764 | ||||||
chr21:44964026
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(90): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.353-3008G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964026 | ||||||
chr21:44964052
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-2982A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964052 | ||||||
chr21:44964078
|
A | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(91): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.353-2956A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964078 | ||||||
chr21:44964226
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.353-2808C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964226 | ||||||
chr21:44964306
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.353-2728A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964306 | ||||||
chr21:44964375
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(2): Show | 6 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-2659C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964375 | ||||||
chr21:44964390
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.353-2644C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964390 | ||||||
chr21:44964403
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-2631T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964403 | ||||||
chr21:44964418
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.353-2616A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964418 | ||||||
chr21:44964451
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.353-2583G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964451 | ||||||
chr21:44964493
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-2541C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964493 | ||||||
chr21:44964543
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.353-2491G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964543 | ||||||
chr21:44964619
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.353-2415C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964619 | ||||||
chr21:44964728
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-2306G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964728 | ||||||
chr21:44964779
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.353-2255G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964779 | ||||||
chr21:44964845
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.353-2189C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964845 | ||||||
chr21:44964892
|
A | G | 1 | a0001c0001t0001g0030 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.353-2142A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964892 | ||||||
chr21:44964897
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.353-2137G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44964897 | ||||||
chr21:44965101
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.353-1933A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965101 | ||||||
chr21:44965132
|
C | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-1902C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965132 | ||||||
chr21:44965138
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-1896G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965138 | ||||||
chr21:44965148
|
A | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-1886A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965148 | ||||||
chr21:44965349
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.353-1685C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965349 | ||||||
chr21:44965350
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.353-1684C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965350 | ||||||
chr21:44965549
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.353-1485A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965549 | ||||||
chr21:44965838
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.353-1196G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965838 | ||||||
chr21:44965967
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.353-1067C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44965967 | ||||||
chr21:44966126
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-908G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966126 | ||||||
chr21:44966141
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-893C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966141 | ||||||
chr21:44966142
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-892G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966142 | ||||||
chr21:44966143
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-891G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966143 | ||||||
chr21:44966144
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-890G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966144 | ||||||
chr21:44966147
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-887G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966147 | ||||||
chr21:44966148
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-886G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966148 | ||||||
chr21:44966151
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-883A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966151 | ||||||
chr21:44966152
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-882G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966152 | ||||||
chr21:44966153
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-881G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966153 | ||||||
chr21:44966154
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-880G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966154 | ||||||
chr21:44966155
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-879T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966155 | ||||||
chr21:44966156
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-878G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966156 | ||||||
chr21:44966157
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-877G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966157 | ||||||
chr21:44966158
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-876G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966158 | ||||||
chr21:44966159
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-875C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966159 | ||||||
chr21:44966163
|
T | TCTTCACC others(7): Show |
1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353-870_353-869ins others(14): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr21 | 44966163 | |||||
chr21:44966218
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.353-816C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966218 | ||||||
chr21:44966251
|
G | A | 1 | a0001c0001t0001g0013 | 3 | HG02683.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.353-783G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966251 | ||||||
chr21:44966291
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353-743G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966291 | ||||||
chr21:44966533
|
C | T | 4 | a0003c0003t0001g0016a0003c0003t0001g0216a0003c0003t0001g0217others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-501C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966533 | ||||||
chr21:44966563
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.353-471C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966563 | ||||||
chr21:44966743
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-291G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966743 | ||||||
chr21:44966891
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185 | 4 | HG02630.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.353-143C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44966891 | ||||||
chr21:44967022
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.353-12C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 3/5 | chr21 | 44967022 | ||||||
chr21:44967191
|
C | T | 28 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(25): Show | 39 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.500+10C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967191 | ||||||
chr21:44967192
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.500+11G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967192 | ||||||
chr21:44967193
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.500+12G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967193 | ||||||
chr21:44967237
|
A | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+56A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967237 | ||||||
chr21:44967354
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.500+173C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967354 | ||||||
chr21:44967363
|
C | G | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.500+182C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967363 | ||||||
chr21:44967370
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0035others(24): Show | 39 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.500+189G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967370 | ||||||
chr21:44967437
|
C | T | 34 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(31): Show | 45 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.500+256C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967437 | ||||||
chr21:44967491
|
C | T | 4 | a0003c0003t0001g0016a0003c0003t0001g0216a0003c0003t0001g0217others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.500+310C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967491 | ||||||
chr21:44967592
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0127a0001c0001t0001g0202 | 3 | HG01515.hp1 HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.500+411G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967592 | ||||||
chr21:44967665
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.500+484C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967665 | ||||||
chr21:44967711
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+530G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967711 | ||||||
chr21:44967749
|
C | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+568C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967749 | ||||||
chr21:44967813
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+632C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967813 | ||||||
chr21:44967839
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+658G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967839 | ||||||
chr21:44967853
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.500+672C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967853 | ||||||
chr21:44967854
|
G | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+673G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44967854 | ||||||
chr21:44968029
|
GGGCCC | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+849_500+853del others(5): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968029 | ||||||
chr21:44968044
|
G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.500+863G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968044 | ||||||
chr21:44968082
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.500+901C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968082 | ||||||
chr21:44968150
|
C | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 8 | HG01167.hp1 HG02257.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.500+969C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968150 | ||||||
chr21:44968241
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0105a0001c0001t0001g0127others(1): Show | 4 | HG01515.hp1 HG02735.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+1060C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968241 | ||||||
chr21:44968467
|
A | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+1286A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968467 | ||||||
chr21:44968522
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+1341A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968522 | ||||||
chr21:44968610
|
C | T | 1 | a0004c0004t0001g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.500+1429C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968610 | ||||||
chr21:44968693
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.500+1512G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968693 | ||||||
chr21:44968694
|
G | C | 37 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(34): Show | 50 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.500+1513G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968694 | ||||||
chr21:44968734
|
CATTT | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+1554_500+1557d others(6): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968734 | ||||||
chr21:44968750
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.500+1569G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968750 | ||||||
chr21:44968753
|
C | CT | 48 | a0001c0001t0001g0030a0001c0001t0001g0070a0001c0001t0001g0094others(45): Show | 62 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.500+1589dupT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44968753 | |||||
chr21:44968807
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0116 | 6 | NA18969.hp1 NA19007.hp1 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+1626G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968807 | ||||||
chr21:44968813
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.500+1632G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968813 | ||||||
chr21:44968840
|
G | T | 32 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(29): Show | 45 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.500+1659G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968840 | ||||||
chr21:44968893
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 7 | HG01167.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+1712A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968893 | ||||||
chr21:44968938
|
G | A | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | NA18747.hp1 NA18955.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.500+1757G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44968938 | ||||||
chr21:44969034
|
T | C | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | NA18747.hp1 NA18955.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.500+1853T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969034 | ||||||
chr21:44969088
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.500+1907T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969088 | ||||||
chr21:44969102
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.500+1921C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969102 | ||||||
chr21:44969229
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.500+2048C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969229 | ||||||
chr21:44969232
|
C | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(8): Show | 13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.500+2051C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969232 | ||||||
chr21:44969239
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.500+2058A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969239 | ||||||
chr21:44969274
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.500+2093C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969274 | ||||||
chr21:44969297
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0041others(16): Show | 24 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.500+2116A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969297 | ||||||
chr21:44969453
|
T | C | 1 | a0002c0002t0001g0213 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.500+2272T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969453 | ||||||
chr21:44969496
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.500+2315A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969496 | ||||||
chr21:44969661
|
C | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+2480C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969661 | ||||||
chr21:44969667
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.500+2486A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969667 | ||||||
chr21:44969686
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.500+2505A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969686 | ||||||
chr21:44969699
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0175 | 2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.500+2518C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969699 | ||||||
chr21:44969740
|
C | T | 1 | a0003c0003t0001g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.500+2559C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969740 | ||||||
chr21:44969749
|
AT | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+2570delT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44969749 | |||||
chr21:44969800
|
C | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.500+2619C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969800 | ||||||
chr21:44969837
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.500+2656C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969837 | ||||||
chr21:44969870
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0144others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+2689G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969870 | ||||||
chr21:44969936
|
C | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+2755C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44969936 | ||||||
chr21:44969945
|
GA | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.500+2766delA | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44969945 | |||||
chr21:44970067
|
C | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(17): Show | 31 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.500+2886C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970067 | ||||||
chr21:44970070
|
GA | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(3): Show | 7 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+2890delA | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970070 | ||||||
chr21:44970085
|
C | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+2904C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970085 | ||||||
chr21:44970098
|
G | GT | 3 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185 | 4 | HG02630.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+2917_500+2918i others(3): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970098 | ||||||
chr21:44970099
|
A | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.500+2918A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970099 | ||||||
chr21:44970118
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.500+2937C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970118 | ||||||
chr21:44970154
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.500+2973G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970154 | ||||||
chr21:44970267
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-2930C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970267 | ||||||
chr21:44970357
|
GTTC | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-2837_501-2835d others(5): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44970357 | |||||
chr21:44970381
|
C | T | 1 | a0001c0001t0001g0041 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.501-2816C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970381 | ||||||
chr21:44970505
|
C | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185 | 4 | HG02630.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-2692C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970505 | ||||||
chr21:44970507
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-2690C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970507 | ||||||
chr21:44970508
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-2689T>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970508 | ||||||
chr21:44970677
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-2520G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970677 | ||||||
chr21:44970851
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-2346C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970851 | ||||||
chr21:44970856
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-2341G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970856 | ||||||
chr21:44970899
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-2298C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970899 | ||||||
chr21:44970900
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-2297T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44970900 | ||||||
chr21:44971025
|
G | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0020others(19): Show | 28 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.501-2172G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971025 | ||||||
chr21:44971042
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.501-2155G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971042 | ||||||
chr21:44971072
|
G | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0199 | 2 | NA18973.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.501-2125G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971072 | ||||||
chr21:44971141
|
G | GCCTCCTG others(52): Show |
1 | a0001c0001t0001g0106 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.501-2035_501-2034i others(61): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44971141 | |||||
chr21:44971141
|
G | GCCTCCTG others(54): Show |
185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 262 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.501-2034_501-2033i others(63): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44971141 | |||||
chr21:44971172
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.501-2025G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971172 | ||||||
chr21:44971194
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.501-2003C>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971194 | ||||||
chr21:44971194
|
C | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(3): Show | 7 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-2003C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971194 | ||||||
chr21:44971223
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.501-1974G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971223 | ||||||
chr21:44971302
|
G | A | 2 | a0004c0004t0001g0219a0004c0004t0001g0227 | 2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.501-1895G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971302 | ||||||
chr21:44971342
|
C | T | 43 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0044others(40): Show | 57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.501-1855C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971342 | ||||||
chr21:44971390
|
GT | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-1806delT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971390 | ||||||
chr21:44971452
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-1745G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971452 | ||||||
chr21:44971454
|
A | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.501-1743A>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971454 | ||||||
chr21:44971485
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-1712A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971485 | ||||||
chr21:44971650
|
A | AC | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-1544dupC | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44971650 | |||||
chr21:44971683
|
A | AG | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.501-1511dupG | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44971683 | |||||
chr21:44971699
|
A | AG | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.501-1494dupG | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44971699 | |||||
chr21:44971704
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.501-1493C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971704 | ||||||
chr21:44971720
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.501-1477T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971720 | ||||||
chr21:44971736
|
C | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(3): Show | 7 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-1461C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971736 | ||||||
chr21:44971738
|
G | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-1459G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971738 | ||||||
chr21:44971857
|
G | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.501-1340G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971857 | ||||||
chr21:44971940
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.501-1257G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44971940 | ||||||
chr21:44972086
|
T | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.501-1111T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972086 | ||||||
chr21:44972116
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.501-1081C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972116 | ||||||
chr21:44972150
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.501-1047C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972150 | ||||||
chr21:44972167
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.501-1030C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972167 | ||||||
chr21:44972294
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-903G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972294 | ||||||
chr21:44972330
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-867G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972330 | ||||||
chr21:44972374
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0098others(1): Show | 9 | NA18940.hp2 NA18941.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-823G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972374 | ||||||
chr21:44972376
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.501-821G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972376 | ||||||
chr21:44972379
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.501-818C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972379 | ||||||
chr21:44972383
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0200 | 3 | HG02258.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.501-814C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972383 | ||||||
chr21:44972427
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.501-770C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972427 | ||||||
chr21:44972541
|
C | T | 1 | a0002c0002t0001g0205 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.501-656C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972541 | ||||||
chr21:44972565
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.501-632G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972565 | ||||||
chr21:44972590
|
C | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0134a0003c0003t0001g0029others(10): Show | 14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.501-607C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972590 | ||||||
chr21:44972687
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0143others(4): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-510C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972687 | ||||||
chr21:44972713
|
G | T | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.501-484G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972713 | ||||||
chr21:44972739
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(2): Show | 6 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-458G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972739 | ||||||
chr21:44972945
|
C | CGCCGTCA others(34): Show |
1 | a0001c0001t0001g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.501-250_501-249ins others(41): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44972945 | |||||
chr21:44972945
|
C | CGCGGTCA others(34): Show |
50 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0043others(47): Show | 65 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.501-213_501-173dup others(41): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44972945 | |||||
chr21:44972960
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.501-237G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44972960 | ||||||
chr21:44972960
|
G | GTCAGGCA others(35): Show |
1 | a0001c0001t0001g0100 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.501-207_501-206ins others(42): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44972960 | |||||
chr21:44972960
|
G | GTCAGGCA others(34): Show |
142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.501-197_501-196ins others(41): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr21 | 44972960 | |||||
chr21:44973081
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.501-116G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44973081 | ||||||
chr21:44973156
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.501-41G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44973156 | ||||||
chr21:44973175
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.501-22C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 4/5 | chr21 | 44973175 | ||||||
chr21:44973319
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.569+54T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973319 | ||||||
chr21:44973319
|
TGCCCACC others(36): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0098 | 5 | NA18940.hp2 NA18945.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+83_569+125delA others(42): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973319 | |||||
chr21:44973358
|
ACCCCGCC others(294): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.569+127_569+427del | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973358 | |||||
chr21:44973391
|
G | A | 1 | a0002c0002t0001g0228 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.569+126G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973391 | ||||||
chr21:44973392
|
A | AGTGCCCT others(552): Show |
3 | a0003c0003t0001g0016a0003c0003t0001g0216a0003c0003t0001g0218 | 5 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+243_569+244ins others(559): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973392 | |||||
chr21:44973392
|
A | T | 1 | a0002c0002t0001g0228 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.569+127A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973392 | ||||||
chr21:44973423
|
GTTCAGCT others(165): Show |
G | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.569+169_569+340del | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973423 | |||||
chr21:44973434
|
A | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0144others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+169A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973434 | ||||||
chr21:44973435
|
T | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0144others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+170T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973435 | ||||||
chr21:44973435
|
TGTGCCCT others(165): Show |
T | 24 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0020others(21): Show | 31 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.569+212_569+383del | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973435 | |||||
chr21:44973444
|
A | ACCCCGCC others(553): Show |
1 | a0003c0003t0001g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.569+243_569+244ins others(560): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973444 | |||||
chr21:44973444
|
ACCCCGCC others(122): Show |
A | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0144others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+201_569+329del | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973444 | |||||
chr21:44973477
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.569+212G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973477 | ||||||
chr21:44973478
|
A | AGTGCCCT others(552): Show |
1 | a0002c0002t0001g0214 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.569+243_569+244ins others(559): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973478 | |||||
chr21:44973478
|
A | AGTGCCCT others(466): Show |
10 | a0002c0002t0001g0230a0002c0002t0001g0232a0004c0004t0001g0017others(7): Show | 13 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.569+243_569+244ins others(473): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973478 | |||||
chr21:44973478
|
A | AGTGCCCT others(466): Show |
13 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(10): Show | 21 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.569+243_569+244ins others(473): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973478 | |||||
chr21:44973478
|
A | AGTGCCCT others(552): Show |
1 | a0004c0004t0001g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.569+243_569+244ins others(559): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973478 | |||||
chr21:44973478
|
A | AGTGCCCT others(466): Show |
1 | a0002c0002t0001g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.569+243_569+244ins others(473): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973478 | |||||
chr21:44973478
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.569+213A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973478 | ||||||
chr21:44973478
|
AGTGCCCT others(79): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.569+222_569+307del others(86): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973478 | |||||
chr21:44973487
|
ACCCCGCC others(79): Show |
A | 104 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 160 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.569+330_569+415del others(86): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973487 | |||||
chr21:44973509
|
A | G | 59 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0134others(56): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.569+244A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973509 | ||||||
chr21:44973520
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.569+255G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973520 | ||||||
chr21:44973521
|
A | AGTGCCCT others(423): Show |
1 | a0004c0004t0001g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.569+286_569+287ins others(430): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973521 | |||||
chr21:44973521
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.569+256A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973521 | ||||||
chr21:44973530
|
ACCCCGCC others(36): Show |
A | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+287_569+329del others(43): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973530 | |||||
chr21:44973552
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.569+287G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973552 | ||||||
chr21:44973552
|
GTTCAGCT others(36): Show |
G | 19 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0134others(16): Show | 21 | HG01167.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.569+298_569+340del others(43): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973552 | |||||
chr21:44973563
|
A | G | 33 | a0001c0001t0001g0186a0002c0002t0001g0002a0002c0002t0001g0204others(30): Show | 46 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.569+298A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973563 | ||||||
chr21:44973564
|
T | A | 33 | a0001c0001t0001g0186a0002c0002t0001g0002a0002c0002t0001g0204others(30): Show | 46 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.569+299T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973564 | ||||||
chr21:44973564
|
T | TGTGCCCT others(36): Show |
1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.569+307_569+308ins others(43): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973564 | |||||
chr21:44973573
|
G | A | 34 | a0001c0001t0001g0018a0001c0001t0001g0186a0002c0002t0001g0002others(31): Show | 48 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.569+308G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973573 | ||||||
chr21:44973573
|
GCCCCGCC others(36): Show |
G | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0156 | 3 | HG02602.hp1 HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.569+330_569+372del others(43): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44973573 | |||||
chr21:44973595
|
A | G | 36 | a0001c0001t0001g0018a0001c0001t0001g0145a0001c0001t0001g0200others(33): Show | 50 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.569+330A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973595 | ||||||
chr21:44973603
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.569+338C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973603 | ||||||
chr21:44973606
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.569+341G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973606 | ||||||
chr21:44973607
|
A | T | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.569+342A>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973607 | ||||||
chr21:44973616
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.569+351A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973616 | ||||||
chr21:44973638
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.569+373G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973638 | ||||||
chr21:44973649
|
A | G | 2 | a0001c0001t0001g0145a0004c0004t0001g0222 | 2 | HG01952.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.569+384A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973649 | ||||||
chr21:44973650
|
T | A | 2 | a0001c0001t0001g0145a0004c0004t0001g0222 | 2 | HG01952.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.569+385T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973650 | ||||||
chr21:44973659
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0144others(3): Show | 6 | HG01952.hp1 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+394G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973659 | ||||||
chr21:44973692
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.569+427G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973692 | ||||||
chr21:44973771
|
C | T | 36 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(33): Show | 48 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.569+506C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973771 | ||||||
chr21:44973776
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+511G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973776 | ||||||
chr21:44973876
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.569+611G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44973876 | ||||||
chr21:44974010
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.569+745C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974010 | ||||||
chr21:44974058
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.569+793G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974058 | ||||||
chr21:44974150
|
T | C | 76 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0039others(73): Show | 93 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.569+885T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974150 | ||||||
chr21:44974217
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.569+952A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974217 | ||||||
chr21:44974223
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.569+958G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974223 | ||||||
chr21:44974249
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 251 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.569+984T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974249 | ||||||
chr21:44974252
|
G | GT | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.569+989dupT | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44974252 | |||||
chr21:44974260
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.569+995G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974260 | ||||||
chr21:44974329
|
GCTGT | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(8): Show | 14 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.569+1069_569+1072d others(6): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44974329 | |||||
chr21:44974353
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.569+1088A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974353 | ||||||
chr21:44974355
|
G | A | 2 | a0001c0001t0001g0200a0006c0006t0001g0137 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+1090G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974355 | ||||||
chr21:44974367
|
G | C | 45 | a0001c0001t0001g0048a0001c0001t0001g0072a0001c0001t0001g0134others(42): Show | 57 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.569+1102G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974367 | ||||||
chr21:44974372
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0138a0001c0001t0001g0140others(3): Show | 7 | HG01167.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.569+1107G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974372 | ||||||
chr21:44974544
|
C | T | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.569+1279C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974544 | ||||||
chr21:44974651
|
C | T | 30 | a0001c0001t0001g0200a0002c0002t0001g0002a0002c0002t0001g0204others(27): Show | 41 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.569+1386C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974651 | ||||||
chr21:44974667
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.569+1402G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974667 | ||||||
chr21:44974682
|
C | T | 5 | a0004c0004t0001g0042a0004c0004t0001g0220a0004c0004t0001g0222others(2): Show | 6 | HG01361.hp1 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+1417C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974682 | ||||||
chr21:44974709
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0144 | 3 | HG02258.hp1 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.569+1444G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974709 | ||||||
chr21:44974717
|
TTGTGTTT others(15): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.569+1455_569+1476d others(24): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44974717 | |||||
chr21:44974763
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.569+1498T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974763 | ||||||
chr21:44974876
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.569+1611C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974876 | ||||||
chr21:44974917
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.569+1652C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44974917 | ||||||
chr21:44975103
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01346.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.570-1577C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975103 | ||||||
chr21:44975119
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.570-1561C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975119 | ||||||
chr21:44975215
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.570-1465C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975215 | ||||||
chr21:44975260
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0144 | 3 | HG02258.hp1 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.570-1420C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975260 | ||||||
chr21:44975440
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.570-1240C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975440 | ||||||
chr21:44975441
|
C | T | 44 | a0002c0002t0001g0002a0002c0002t0001g0204a0002c0002t0001g0205others(41): Show | 58 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.570-1239C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975441 | ||||||
chr21:44975528
|
C | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0035others(33): Show | 48 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.570-1152C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975528 | ||||||
chr21:44975757
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.570-923C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975757 | ||||||
chr21:44975876
|
G | T | 1 | a0002c0002t0001g0228 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.570-804G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975876 | ||||||
chr21:44975957
|
G | A | 5 | a0004c0004t0001g0042a0004c0004t0001g0220a0004c0004t0001g0222others(2): Show | 6 | HG01361.hp1 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.570-723G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44975957 | ||||||
chr21:44976126
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0134 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.570-554G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976126 | ||||||
chr21:44976142
|
G | C | 57 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0043others(54): Show | 73 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.570-538G>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976142 | ||||||
chr21:44976159
|
C | G | 1 | a0001c0001t0001g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.570-521C>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976159 | ||||||
chr21:44976164
|
T | A | 1 | a0003c0003t0001g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.570-516T>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976164 | ||||||
chr21:44976275
|
A | AGGCTCTC others(7): Show |
1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570-390_570-377dup others(14): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44976275 | |||||
chr21:44976275
|
AGGCTCTC | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 56 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.570-383_570-377del others(7): Show |
SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr21 | 44976275 | |||||
chr21:44976325
|
T | C | 1 | a0004c0004t0001g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.570-355T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976325 | ||||||
chr21:44976351
|
T | C | 56 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0043others(53): Show | 72 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.570-329T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976351 | ||||||
chr21:44976386
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.570-294G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976386 | ||||||
chr21:44976407
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.570-273G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976407 | ||||||
chr21:44976416
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570-264A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976416 | ||||||
chr21:44976452
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0145 | 2 | HG02056.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.570-228C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976452 | ||||||
chr21:44976537
|
G | A | 1 | a0003c0003t0001g0053 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.570-143G>A | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976537 | ||||||
chr21:44976560
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(1): Show | 5 | HG01109.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.570-120T>C | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976560 | ||||||
chr21:44976567
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570-113C>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976567 | ||||||
chr21:44976631
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570-49A>G | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976631 | ||||||
chr21:44976635
|
G | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0185others(1): Show | 5 | HG01109.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.570-45G>T | SLX9 | ENSG00000160256.14 | transcript | ENST00000291634.11 | protein_coding | 5/5 | chr21 | 44976635 |