Variant report

Variant	rs7012905
Chromosome Location	chr8:11382177-11382178
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs6990222	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6990576	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6992453	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6992979	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6993123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6993135	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6993287	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6994857	1.00[AMR][1000 genomes]
rs7008451	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7012605	1.00[AFR][1000 genomes]
rs7012615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7831602	1.00[AMR][1000 genomes]
rs7831922	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022074	chr8:11292256-11394526	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11372200-11386000	Weak transcription	Spleen	Spleen
2	chr8:11376600-11382200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:11376800-11382200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:11380800-11385400	Genic enhancers	Primary B cells from peripheral blood	blood
5	chr8:11381800-11382600	Enhancers	Primary B cells from cord blood	blood
6	chr8:11381800-11382800	Flanking Active TSS	Dnd41	blood
7	chr8:11382000-11382200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:11382000-11382200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:11382000-11382200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:11382000-11382400	Flanking Active TSS	HUVEC	blood vessel
11	chr8:11382000-11382400	Active TSS	NHLF	lung
12	chr8:11382000-11382600	Flanking Active TSS	GM12878-XiMat	blood
13	chr8:11382000-11382600	Enhancers	NHDF-Ad	bronchial
14	chr8:11382000-11382600	Flanking Active TSS	Osteobl	bone
15	chr8:11382000-11382800	Enhancers	Thymus	Thymus
16	chr8:11382000-11383400	Enhancers	Fetal Thymus	thymus

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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