Variant report
Variant | rs7910281 |
---|---|
Chromosome Location | chr10:116652258-116652259 |
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] |
---|---|
rs1116508 | 1.00[EUR][1000 genomes] |
rs11812214 | 1.00[EUR][1000 genomes] |
rs1264777 | 1.00[EUR][1000 genomes] |
rs1264800 | 1.00[EUR][1000 genomes] |
rs1264804 | 1.00[EUR][1000 genomes] |
rs1268462 | 1.00[EUR][1000 genomes] |
rs1268917 | 1.00[EUR][1000 genomes] |
rs17092411 | 1.00[EUR][1000 genomes] |
rs2146804 | 1.00[EUR][1000 genomes] |
rs56844582 | 1.00[EUR][1000 genomes] |
rs56859887 | 1.00[EUR][1000 genomes] |
rs57025690 | 1.00[EUR][1000 genomes] |
rs57196389 | 1.00[AMR][1000 genomes] |
rs57201267 | 1.00[EUR][1000 genomes] |
rs57551865 | 1.00[EUR][1000 genomes] |
rs57627999 | 1.00[EUR][1000 genomes] |
rs57955640 | 1.00[EUR][1000 genomes] |
rs58043949 | 1.00[EUR][1000 genomes] |
rs58167147 | 1.00[EUR][1000 genomes] |
rs58366976 | 1.00[EUR][1000 genomes] |
rs59660416 | 1.00[EUR][1000 genomes] |
rs59919921 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60092663 | 1.00[EUR][1000 genomes] |
rs60163199 | 1.00[EUR][1000 genomes] |
rs60266547 | 1.00[EUR][1000 genomes] |
rs60297453 | 1.00[EUR][1000 genomes] |
rs60410790 | 1.00[EUR][1000 genomes] |
rs60690229 | 1.00[EUR][1000 genomes] |
rs60738938 | 1.00[EUR][1000 genomes] |
rs61207042 | 1.00[EUR][1000 genomes] |
rs61479736 | 1.00[AMR][1000 genomes] |
rs7072302 | 1.00[AMR][1000 genomes] |
rs7087895 | 1.00[EUR][1000 genomes] |
rs7089161 | 1.00[EUR][1000 genomes] |
rs7091595 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7093074 | 1.00[EUR][1000 genomes] |
rs7093407 | 1.00[AMR][1000 genomes] |
rs7093923 | 1.00[EUR][1000 genomes] |
rs7097805 | 1.00[EUR][1000 genomes] |
rs7100519 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7100802 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73357605 | 1.00[EUR][1000 genomes] |
rs73357608 | 1.00[EUR][1000 genomes] |
rs73357614 | 1.00[EUR][1000 genomes] |
rs73357618 | 1.00[EUR][1000 genomes] |
rs73357630 | 1.00[EUR][1000 genomes] |
rs73361960 | 1.00[EUR][1000 genomes] |
rs73361970 | 1.00[EUR][1000 genomes] |
rs73361981 | 1.00[EUR][1000 genomes] |
rs73361987 | 1.00[EUR][1000 genomes] |
rs73363907 | 1.00[EUR][1000 genomes] |
rs73363913 | 1.00[EUR][1000 genomes] |
rs73363916 | 1.00[EUR][1000 genomes] |
rs73367377 | 1.00[EUR][1000 genomes] |
rs73367389 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73368776 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73368780 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73370603 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73370613 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73370694 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73371868 | 1.00[EUR][1000 genomes] |
rs73371874 | 1.00[EUR][1000 genomes] |
rs73371876 | 1.00[EUR][1000 genomes] |
rs73371880 | 1.00[EUR][1000 genomes] |
rs73371883 | 1.00[EUR][1000 genomes] |
rs73371890 | 1.00[EUR][1000 genomes] |
rs73371894 | 1.00[EUR][1000 genomes] |
rs73372634 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73372656 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73372660 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73372663 | 1.00[AMR][1000 genomes] |
rs73372680 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73372689 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73373705 | 1.00[EUR][1000 genomes] |
rs73373708 | 1.00[EUR][1000 genomes] |
rs73373750 | 1.00[EUR][1000 genomes] |
rs73373754 | 1.00[EUR][1000 genomes] |
rs73373756 | 1.00[EUR][1000 genomes] |
rs73373760 | 1.00[EUR][1000 genomes] |
rs73374610 | 1.00[AMR][1000 genomes] |
rs73374614 | 1.00[AMR][1000 genomes] |
rs73374623 | 1.00[AMR][1000 genomes] |
rs73374634 | 1.00[AMR][1000 genomes] |
rs73374677 | 1.00[AMR][1000 genomes] |
rs73374685 | 1.00[AMR][1000 genomes] |
rs7899872 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7907892 | 1.00[EUR][1000 genomes] |
rs7917766 | 1.00[AMR][1000 genomes] |
rs7921195 | 1.00[EUR][1000 genomes] |
rs7921864 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949138 | chr10:116311531-116874477 | Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv1038050 | chr10:116315109-116895719 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
3 | nsv533027 | chr10:116344641-116856352 | Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
4 | esv3435429 | chr10:116394152-117006347 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
5 | nsv831996 | chr10:116601552-116772968 | Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
6 | nsv1039002 | chr10:116643095-116879483 | Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
7 | esv2761634 | chr10:116643095-116879495 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
8 | esv3400350 | chr10:116649212-116653810 | Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:116642200-116655800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |