Variant report

Variant	rs9856164
Chromosome Location	chr3:68105829-68105830
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs35567425	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1009871	chr3:67862617-68312064	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv536583	chr3:67862617-68312064	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1010231	chr3:67894825-68117879	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv999747	chr3:68066423-68188180	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv536584	chr3:68066423-68188180	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1007450	chr3:68094416-68346546	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68103800-68106200	Enhancers	Fetal Intestine Small	intestine
2	chr3:68104200-68106600	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr3:68104800-68106200	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr3:68105000-68106200	Enhancers	Primary T cells from cord blood	blood
5	chr3:68105000-68106200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr3:68105000-68106200	Enhancers	Duodenum Mucosa	Duodenum
7	chr3:68105000-68106600	Enhancers	Primary T cells fromperipheralblood	blood
8	chr3:68105000-68106600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr3:68105000-68106600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:68105000-68109000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr3:68105200-68107000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr3:68105400-68106000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr3:68105400-68106800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr3:68105400-68107000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr3:68105400-68108400	Weak transcription	Fetal Intestine Large	intestine
16	chr3:68105600-68106200	Enhancers	Aorta	Aorta
17	chr3:68105800-68106000	Enhancers	Small Intestine	intestine
18	chr3:68105800-68106800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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