Variant report

Variant	rs7614914
Chromosome Location	chr3:28263431-28263432
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:28261846..28264997-chr3:28280246..28283613,3	K562	blood:

Variant related genes	Relation type
ENSG00000187118	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs11129313	0.82[AFR][1000 genomes]
rs11916111	1.00[ASN][1000 genomes]
rs11916585	1.00[ASN][1000 genomes]
rs11916606	0.97[ASN][1000 genomes]
rs11916686	1.00[ASN][1000 genomes]
rs11918487	1.00[ASN][1000 genomes]
rs11920615	1.00[ASN][1000 genomes]
rs11923769	1.00[ASN][1000 genomes]
rs11926903	1.00[ASN][1000 genomes]
rs11927668	1.00[ASN][1000 genomes]
rs12107183	1.00[ASN][1000 genomes]
rs12107191	1.00[ASN][1000 genomes]
rs12107565	1.00[ASN][1000 genomes]
rs17021208	1.00[ASN][1000 genomes]
rs17021215	1.00[ASN][1000 genomes]
rs17021232	1.00[ASN][1000 genomes]
rs17021238	1.00[ASN][1000 genomes]
rs34692982	0.83[AFR][1000 genomes]
rs35178864	1.00[ASN][1000 genomes]
rs4680746	0.82[AFR][1000 genomes]
rs55940261	1.00[ASN][1000 genomes]
rs56250178	1.00[ASN][1000 genomes]
rs56687471	1.00[ASN][1000 genomes]
rs57267508	1.00[ASN][1000 genomes]
rs57358658	1.00[ASN][1000 genomes]
rs58886943	1.00[ASN][1000 genomes]
rs58899029	1.00[ASN][1000 genomes]
rs60163502	1.00[ASN][1000 genomes]
rs60163709	1.00[ASN][1000 genomes]
rs61479857	1.00[ASN][1000 genomes]
rs61548543	1.00[ASN][1000 genomes]
rs61633201	1.00[ASN][1000 genomes]
rs6778650	1.00[ASN][1000 genomes]
rs6780084	1.00[ASN][1000 genomes]
rs6791708	1.00[ASN][1000 genomes]
rs6792215	0.82[AFR][1000 genomes]
rs6793933	1.00[ASN][1000 genomes]
rs6794980	1.00[ASN][1000 genomes]
rs6795634	1.00[ASN][1000 genomes]
rs6797580	1.00[ASN][1000 genomes]
rs6798101	1.00[ASN][1000 genomes]
rs6802491	1.00[ASN][1000 genomes]
rs6809163	1.00[ASN][1000 genomes]
rs6809917	1.00[ASN][1000 genomes]
rs72898235	1.00[ASN][1000 genomes]
rs73822327	1.00[ASN][1000 genomes]
rs73822555	1.00[ASN][1000 genomes]
rs73823423	1.00[ASN][1000 genomes]
rs73823424	1.00[ASN][1000 genomes]
rs73823425	1.00[ASN][1000 genomes]
rs73823426	1.00[ASN][1000 genomes]
rs73823427	1.00[ASN][1000 genomes]
rs73823429	1.00[ASN][1000 genomes]
rs73823432	1.00[ASN][1000 genomes]
rs73823433	1.00[ASN][1000 genomes]
rs73823434	1.00[ASN][1000 genomes]
rs7610729	1.00[ASN][1000 genomes]
rs7635045	1.00[ASN][1000 genomes]
rs7638878	1.00[ASN][1000 genomes]
rs7639138	1.00[ASN][1000 genomes]
rs9637515	0.81[AFR][1000 genomes]
rs966029	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876648	chr3:28060456-28280965	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	esv3451771	chr3:28262398-28264496	Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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