Variant report

Variant	rs72652067
Chromosome Location	chr4:88326972-88326973
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	YY1	chr4:88326847-88326984	K562	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000249262	TF binding region

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10000196	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10009948	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10023606	0.97[ASN][1000 genomes]
rs10024781	0.92[ASN][1000 genomes]
rs10030035	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10032122	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10084883	0.95[ASN][1000 genomes]
rs12640451	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12640894	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12648665	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12650763	0.95[ASN][1000 genomes]
rs12651034	0.95[ASN][1000 genomes]
rs28366407	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28415220	0.92[ASN][1000 genomes]
rs28437709	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28493315	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs28493566	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28529046	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28535549	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28696943	0.90[ASN][1000 genomes]
rs28712618	0.95[ASN][1000 genomes]
rs28718986	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28762371	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28805573	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34027531	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4411944	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55824708	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56153912	0.97[ASN][1000 genomes]
rs58192677	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67121411	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs68045074	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7665115	0.95[ASN][1000 genomes]
rs7673763	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7677249	0.95[ASN][1000 genomes]
rs7680878	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7690728	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9995987	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9998212	0.81[AMR][1000 genomes];0.97[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	nsv1004518	chr4:88218473-88354403	Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv1002789	chr4:88239340-88606485	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	esv3447453	chr4:88323528-88329828	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88320600-88329400	Weak transcription	Pancreas	Pancrea
2	chr4:88321000-88327400	Weak transcription	Primary B cells from cord blood	blood
3	chr4:88322000-88327600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:88325600-88327000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:88325600-88327600	Weak transcription	Fetal Intestine Large	intestine
6	chr4:88325800-88327800	Weak transcription	Fetal Lung	lung
7	chr4:88326000-88330600	Weak transcription	K562	blood
8	chr4:88326800-88328000	Enhancers	Stomach Mucosa	stomach
9	chr4:88326800-88329600	Enhancers	Duodenum Mucosa	Duodenum

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