Variant report

Variant	rs4264856
Chromosome Location	chr4:79615951-79615952
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:79608933..79617994-chr4:79691426..79702696,23	K562	blood:
2	chr4:79611783..79613882-chr4:79614566..79616143,2	MCF-7	breast:
3	chr4:79613186..79614843-chr4:79614928..79617514,2	K562	blood:
4	chr4:79608764..79617994-chr4:79689698..79699789,21	K562	blood:

Variant related genes	Relation type
ENSG00000260278	Chromatin interaction
ENSG00000138756	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10008008	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10008069	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10084949	0.88[EUR][1000 genomes]
rs1134123	0.89[EUR][1000 genomes]
rs1134124	0.89[EUR][1000 genomes]
rs11724233	0.81[CHB][hapmap]
rs11931947	0.84[EUR][1000 genomes]
rs13101964	0.85[EUR][1000 genomes]
rs13110339	0.88[JPT][hapmap]
rs13133277	0.97[EUR][1000 genomes]
rs1346144	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1346145	0.95[CEU][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1469289	0.88[EUR][1000 genomes]
rs1469290	0.88[EUR][1000 genomes]
rs1532427	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs1582759	0.88[EUR][1000 genomes]
rs1806906	0.80[CEU][hapmap];0.88[EUR][1000 genomes]
rs1834519	0.95[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1966537	0.87[EUR][1000 genomes]
rs2867465	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2867466	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2903578	0.88[EUR][1000 genomes]
rs4074675	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4254805	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs4257676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4321658	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4365753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4472162	0.87[CEU][hapmap];0.85[CHB][hapmap];0.81[JPT][hapmap];0.91[EUR][1000 genomes]
rs4472163	0.87[CEU][hapmap];0.85[CHB][hapmap];0.91[EUR][1000 genomes]
rs4495064	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs4560439	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4619914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6533940	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6533951	0.80[CHB][hapmap]
rs6815367	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6818230	0.97[EUR][1000 genomes]
rs6825593	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6842723	0.80[CHB][hapmap]
rs6855458	0.95[CEU][hapmap];0.97[EUR][1000 genomes]
rs7672208	0.90[EUR][1000 genomes]
rs7677162	0.90[EUR][1000 genomes]
rs7677783	0.81[CEU][hapmap];0.84[JPT][hapmap]
rs7694971	0.90[EUR][1000 genomes]
rs7699519	0.90[EUR][1000 genomes]
rs7699905	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9992088	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009633	chr4:78887573-79652236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79609000-79616000	Enhancers	NHDF-Ad	bronchial
2	chr4:79610000-79616400	Enhancers	Fetal Intestine Large	intestine
3	chr4:79610600-79617800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:79611400-79616200	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:79611800-79616400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:79612200-79616400	Enhancers	Fetal Intestine Small	intestine
7	chr4:79613400-79616000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:79613400-79616600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:79614200-79616200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr4:79614600-79618200	Enhancers	K562	blood

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