Variant report

Variant	rs7870478
Chromosome Location	chr9:2664867-2664868
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs2054073	0.91[EUR][1000 genomes]
rs2063570	1.00[EUR][1000 genomes]
rs2063571	1.00[EUR][1000 genomes]
rs2063572	1.00[EUR][1000 genomes]
rs34003761	0.91[EUR][1000 genomes]
rs34067270	0.91[EUR][1000 genomes]
rs3421	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs34458671	0.91[EUR][1000 genomes]
rs34811022	0.91[EUR][1000 genomes]
rs35774247	0.91[EUR][1000 genomes]
rs56020844	1.00[EUR][1000 genomes]
rs58045872	0.91[EUR][1000 genomes]
rs58589975	0.91[EUR][1000 genomes]
rs59546407	1.00[EUR][1000 genomes]
rs59816438	0.91[EUR][1000 genomes]
rs7034291	0.96[EUR][1000 genomes]
rs7043836	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7043949	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs73640160	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73640161	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73640162	0.96[EUR][1000 genomes]
rs73640163	0.96[EUR][1000 genomes]
rs73640164	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530929	chr9:1998911-2925112	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv529508	chr9:2267812-2684272	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv916750	chr9:2430846-2826706	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv531564	chr9:2452325-2700375	Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv1017581	chr9:2494815-3172020	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv539934	chr9:2494815-3172020	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv892077	chr9:2663639-2690980	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2641400-2668400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr9:2643800-2666800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:2644000-2667200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:2653000-2666600	Weak transcription	Fetal Stomach	stomach
5	chr9:2654200-2666800	Weak transcription	Lung	lung
6	chr9:2656000-2666600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:2656000-2677800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr9:2661800-2666800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr9:2662200-2665000	Enhancers	Right Atrium	heart
10	chr9:2663600-2665000	Enhancers	Brain Angular Gyrus	brain
11	chr9:2663600-2665000	Enhancers	Dnd41	blood
12	chr9:2663800-2665000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr9:2663800-2665000	Enhancers	Right Ventricle	heart
14	chr9:2664000-2665000	Enhancers	Left Ventricle	heart
15	chr9:2664000-2665000	Enhancers	Psoas Muscle	Psoas
16	chr9:2664000-2665000	Enhancers	Spleen	Spleen
17	chr9:2664200-2665000	Enhancers	Ovary	ovary
18	chr9:2664200-2665000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr9:2664600-2665000	Enhancers	Esophagus	oesophagus
20	chr9:2664800-2665000	Weak transcription	Fetal Brain Female	brain
21	chr9:2664800-2665200	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links