Variant report

Variant	rs59211421
Chromosome Location	chr9:17193719-17193720
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs13286174	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935348	1.00[EUR][1000 genomes]
rs16935377	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935382	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935390	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935395	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935397	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935399	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935548	1.00[EUR][1000 genomes]
rs57907512	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58091700	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59274061	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59305778	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59433459	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59453259	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59698728	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59700619	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60401056	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60503811	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60546162	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61562344	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7020252	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7024284	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7025130	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7025248	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7025329	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7029226	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7036370	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7037203	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7847317	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7847327	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7856183	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7856549	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7861471	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv2764141	chr9:16903446-17351711	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv892657	chr9:17008137-17223492	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv892658	chr9:17041557-17532840	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1023525	chr9:17121773-17236072	Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv892659	chr9:17130360-17236376	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv892660	chr9:17134245-17269437	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv892661	chr9:17134245-17532840	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
9	nsv428537	chr9:17146369-17308494	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv613693	chr9:17147191-17710407	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
11	nsv471287	chr9:17165698-17708814	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
12	nsv466269	chr9:17165698-17710407	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
13	nsv892662	chr9:17168867-17329964	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17159800-17195600	Weak transcription	Aorta	Aorta
2	chr9:17179000-17204400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:17187600-17194800	Weak transcription	Liver	Liver
4	chr9:17191600-17195800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:17191600-17207400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:17192000-17194200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr9:17192000-17194200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr9:17192200-17194000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
9	chr9:17193200-17194200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:17193400-17194200	ZNF genes & repeats	Fetal Stomach	stomach
11	chr9:17193400-17195000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr9:17193600-17193800	Enhancers	Pancreas	Pancrea
13	chr9:17193600-17193800	Enhancers	Right Ventricle	heart
14	chr9:17193600-17194000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr9:17193600-17194200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr9:17193600-17194200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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