Variant report

Variant	rs627216
Chromosome Location	chr9:13705568-13705569
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10115052	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10125903	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12339993	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12344708	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12350251	0.87[AMR][1000 genomes]
rs13292780	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34324640	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs496857	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs504659	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs537556	0.86[EUR][1000 genomes]
rs594872	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs611973	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs612828	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs629775	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs648981	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs789583	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs789593	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs789598	0.90[AMR][1000 genomes];0.84[EUR][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	nsv1023684	chr9:13529680-13744602	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv540067	chr9:13529680-13744602	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv892587	chr9:13601074-13732363	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1843958	chr9:13631992-13706651	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv892588	chr9:13667639-13715063	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv1018933	chr9:13669862-13756710	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv892589	chr9:13689066-13715328	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv892590	chr9:13689066-13777299	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13704200-13705600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:13704400-13706600	Enhancers	HSMM	muscle
3	chr9:13705000-13706600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:13705200-13705600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr9:13705200-13705600	Enhancers	Osteobl	bone
6	chr9:13705200-13705800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:13705200-13706200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr9:13705200-13706400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr9:13705200-13706600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:13705200-13706600	Enhancers	Adipose Nuclei	Adipose
11	chr9:13705200-13706600	Enhancers	HSMMtube	muscle
12	chr9:13705200-13706600	Enhancers	NHDF-Ad	bronchial
13	chr9:13705200-13706800	Enhancers	NHLF	lung
14	chr9:13705200-13707400	Enhancers	HUVEC	blood vessel
15	chr9:13705200-13708000	Enhancers	Fetal Muscle Leg	muscle
16	chr9:13705400-13705600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:13705400-13706200	Enhancers	Placenta	Placenta
18	chr9:13705400-13706400	Enhancers	Fetal Lung	lung
19	chr9:13705400-13706400	Enhancers	Left Ventricle	heart
20	chr9:13705400-13706600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:13705400-13706600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:13705400-13706600	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr9:13705400-13706600	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr9:13705400-13708800	Enhancers	NH-A	brain

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