Variant report

Variant	rs4656168
Chromosome Location	chr1:168896526-168896527
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:168894738..168897178-chr1:169075088..169076984,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143153	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10919009	1.00[ASN][1000 genomes]
rs12075363	1.00[ASN][1000 genomes]
rs1322495	1.00[ASN][1000 genomes]
rs1322502	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1322503	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1358949	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1407479	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1570332	1.00[ASN][1000 genomes]
rs1570333	1.00[ASN][1000 genomes]
rs1590286	1.00[ASN][1000 genomes]
rs200577	1.00[ASN][1000 genomes]
rs2065130	1.00[ASN][1000 genomes]
rs2065131	1.00[ASN][1000 genomes]
rs2146199	1.00[ASN][1000 genomes]
rs2146202	1.00[ASN][1000 genomes]
rs2146203	1.00[ASN][1000 genomes]
rs2419389	1.00[ASN][1000 genomes]
rs2419396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2419685	1.00[ASN][1000 genomes]
rs2900886	1.00[ASN][1000 genomes]
rs2984603	1.00[ASN][1000 genomes]
rs2984605	1.00[ASN][1000 genomes]
rs2984606	1.00[ASN][1000 genomes]
rs2984608	1.00[ASN][1000 genomes]
rs2984609	1.00[ASN][1000 genomes]
rs2984610	1.00[ASN][1000 genomes]
rs2984612	1.00[ASN][1000 genomes]
rs3007391	1.00[ASN][1000 genomes]
rs3007398	1.00[ASN][1000 genomes]
rs61801631	1.00[ASN][1000 genomes]
rs61801632	1.00[ASN][1000 genomes]
rs61801637	1.00[ASN][1000 genomes]
rs61801655	1.00[ASN][1000 genomes]
rs61801656	1.00[ASN][1000 genomes]
rs6427154	1.00[ASN][1000 genomes]
rs6670610	1.00[ASN][1000 genomes]
rs6681955	1.00[ASN][1000 genomes]
rs6686910	1.00[ASN][1000 genomes]
rs704837	1.00[ASN][1000 genomes]
rs7513128	1.00[ASN][1000 genomes]
rs7541615	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7554392	0.87[AFR][1000 genomes]
rs857632	1.00[ASN][1000 genomes]
rs857634	1.00[ASN][1000 genomes]
rs857636	1.00[ASN][1000 genomes]
rs857638	1.00[ASN][1000 genomes]
rs857639	1.00[ASN][1000 genomes]
rs857640	1.00[ASN][1000 genomes]
rs857642	1.00[ASN][1000 genomes]
rs857644	1.00[ASN][1000 genomes]
rs911892	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs968047	1.00[ASN][1000 genomes]
rs971411	0.87[AFR][1000 genomes];1.00[ASN][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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168896400-168901600	Weak transcription	Fetal Heart	heart

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