Variant report
Variant | rs72828851 |
---|---|
Chromosome Location | chr2:111492665-111492666 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs13421709 | 0.86[ASN][1000 genomes] |
rs13426054 | 0.83[ASN][1000 genomes] |
rs17041539 | 0.82[EUR][1000 genomes] |
rs17041553 | 0.82[EUR][1000 genomes] |
rs17041554 | 0.82[EUR][1000 genomes] |
rs17041555 | 0.82[EUR][1000 genomes] |
rs17041561 | 0.82[EUR][1000 genomes] |
rs28452164 | 1.00[EUR][1000 genomes] |
rs34026418 | 0.82[EUR][1000 genomes] |
rs3817265 | 0.82[EUR][1000 genomes] |
rs4255970 | 1.00[EUR][1000 genomes] |
rs55682108 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs55780486 | 0.82[EUR][1000 genomes] |
rs55849112 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs55857945 | 1.00[EUR][1000 genomes] |
rs55875504 | 1.00[EUR][1000 genomes] |
rs55875530 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs55927063 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs55928449 | 0.82[AFR][1000 genomes] |
rs56010803 | 0.82[EUR][1000 genomes] |
rs56031628 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs56062220 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56110941 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56146538 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56165253 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56169320 | 0.82[EUR][1000 genomes] |
rs56177778 | 1.00[EUR][1000 genomes] |
rs56181028 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56202720 | 0.86[ASN][1000 genomes] |
rs56238325 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs56260092 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56272335 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56281800 | 0.82[EUR][1000 genomes] |
rs56289191 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56320021 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs57101781 | 0.82[EUR][1000 genomes] |
rs57318054 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs57847126 | 0.82[EUR][1000 genomes] |
rs57862073 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58054304 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs58569659 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs58588523 | 1.00[EUR][1000 genomes] |
rs59258102 | 1.00[EUR][1000 genomes] |
rs59413237 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs60185821 | 0.82[EUR][1000 genomes] |
rs60357733 | 1.00[EUR][1000 genomes] |
rs61124407 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61376946 | 0.82[EUR][1000 genomes] |
rs61637608 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs66616139 | 1.00[EUR][1000 genomes] |
rs68130860 | 0.83[ASN][1000 genomes] |
rs72828836 | 0.88[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs72828838 | 0.88[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs72828843 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72828844 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72828845 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72828846 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72828847 | 0.83[ASN][1000 genomes] |
rs72828848 | 0.85[ASN][1000 genomes] |
rs72828849 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72828850 | 1.00[ASN][1000 genomes] |
rs72828852 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72828854 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72828856 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72828857 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72828859 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72828861 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830976 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830979 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830980 | 1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72830982 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830984 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830985 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830986 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830989 | 1.00[EUR][1000 genomes] |
rs72830990 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72830993 | 1.00[EUR][1000 genomes] |
rs72830995 | 0.92[EUR][1000 genomes] |
rs72830997 | 1.00[EUR][1000 genomes] |
rs72831000 | 1.00[EUR][1000 genomes] |
rs72832803 | 1.00[EUR][1000 genomes] |
rs72832804 | 1.00[EUR][1000 genomes] |
rs72832809 | 1.00[EUR][1000 genomes] |
rs72832810 | 1.00[EUR][1000 genomes] |
rs72832813 | 1.00[EUR][1000 genomes] |
rs72832815 | 1.00[EUR][1000 genomes] |
rs72832816 | 1.00[EUR][1000 genomes] |
rs72832817 | 1.00[EUR][1000 genomes] |
rs72832818 | 1.00[EUR][1000 genomes] |
rs72832820 | 0.82[EUR][1000 genomes] |
rs72832821 | 0.82[EUR][1000 genomes] |
rs72832822 | 0.82[EUR][1000 genomes] |
rs72832824 | 0.82[EUR][1000 genomes] |
rs72832826 | 0.82[EUR][1000 genomes] |
rs72832828 | 0.82[EUR][1000 genomes] |
rs72832837 | 0.82[EUR][1000 genomes] |
rs72832838 | 0.82[EUR][1000 genomes] |
rs72832839 | 0.82[EUR][1000 genomes] |
rs72832841 | 0.82[EUR][1000 genomes] |
rs72832842 | 0.82[EUR][1000 genomes] |
rs72832843 | 0.82[EUR][1000 genomes] |
rs72832846 | 0.82[EUR][1000 genomes] |
rs73954660 | 0.87[AFR][1000 genomes] |
rs73956436 | 0.81[AFR][1000 genomes] |
rs73956443 | 0.85[AFR][1000 genomes] |
rs73956448 | 0.82[AFR][1000 genomes] |
rs73956450 | 0.81[AFR][1000 genomes] |
rs73956451 | 0.81[AFR][1000 genomes] |
rs977406 | 0.82[EUR][1000 genomes] |
rs981196 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv874838 | chr2:111376870-112046226 | Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
2 | nsv874839 | chr2:111400934-111868010 | Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv1008758 | chr2:111415136-111626467 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv535890 | chr2:111415136-111626467 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
5 | nsv997829 | chr2:111486961-111780537 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:111491200-111492800 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
2 | chr2:111491400-111493000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr2:111491400-111493200 | Weak transcription | Lung | lung |
4 | chr2:111491600-111492800 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
5 | chr2:111491600-111493000 | Weak transcription | H1 Cell Line | embryonic stem cell |
6 | chr2:111491800-111493600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
7 | chr2:111492400-111493000 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
8 | chr2:111492400-111493200 | Bivalent Enhancer | iPS-20b Cell Line | embryonic stem cell |
9 | chr2:111492400-111493200 | Bivalent Enhancer | HepG2 | liver |
10 | chr2:111492400-111493400 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
11 | chr2:111492400-111493400 | Enhancers | H9 Cell Line | embryonic stem cell |
12 | chr2:111492400-111493600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
13 | chr2:111492400-111493800 | Bivalent Enhancer | iPS-18 Cell Line | embryonic stem cell |
14 | chr2:111492600-111493200 | Bivalent Enhancer | HUES6 Cell Line | embryonic stem cell |