Variant report

Variant	rs7693117
Chromosome Location	chr4:76996981-76996982
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr4:76996860-76997060	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
ART3	TF binding region

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10019066	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10025961	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10030471	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10433952	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12499668	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12510239	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12511357	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12511359	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13106039	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28484974	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28601861	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28647509	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35353995	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4404571	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4621456	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55813915	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55964684	0.80[AFR][1000 genomes]
rs56054611	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60282049	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60431104	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532167	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532168	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532169	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532170	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67194908	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67308118	0.96[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67413521	0.83[AFR][1000 genomes]
rs67687266	0.84[ASN][1000 genomes]
rs6857378	0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7666094	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7671170	0.84[ASN][1000 genomes]
rs7671209	0.80[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7676234	0.84[ASN][1000 genomes]
rs7679689	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7684879	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7685390	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7692605	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7693693	0.97[ASN][1000 genomes]
rs9990658	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9998233	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529613	chr4:76654941-77081576	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1004627	chr4:76793910-76999584	Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv1009047	chr4:76989180-77077885	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76995400-76997000	Enhancers	Brain Angular Gyrus	brain
2	chr4:76995600-76997000	Enhancers	Brain Substantia Nigra	brain
3	chr4:76995600-76999400	Active TSS	Psoas Muscle	Psoas
4	chr4:76995600-77000800	Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr4:76995800-76997000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:76995800-76997000	Enhancers	Fetal Heart	heart
7	chr4:76995800-76997000	Active TSS	Left Ventricle	heart
8	chr4:76995800-76998200	Active TSS	Skeletal Muscle Male	skeletal muscle
9	chr4:76995800-76999000	Active TSS	Right Ventricle	heart
10	chr4:76996400-76997000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr4:76996400-76997000	Enhancers	Fetal Brain Male	brain
12	chr4:76996400-76999000	Weak transcription	HSMMtube	muscle
13	chr4:76996800-76997000	Enhancers	Brain Anterior Caudate	brain
14	chr4:76996800-76997000	Enhancers	Brain Cingulate Gyrus	brain

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