Variant report

Variant	rs59390914
Chromosome Location	chr11:74954168-74954169
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:74953050..74955146-chr11:75048496..75050415,2	K562	blood:
2	chr11:74920713..74922645-chr11:74953043..74955609,2	MCF-7	breast:
3	chr11:74640083..74642436-chr11:74952777..74954746,3	MCF-7	breast:
4	chr11:74952768..74954538-chr11:74955270..74959114,3	K562	blood:
5	chr11:74659830..74661713-chr11:74952303..74954332,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000118363	Chromatin interaction
ENSG00000166435	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12721494	0.84[EUR][1000 genomes]
rs17133815	0.92[EUR][1000 genomes]
rs17133831	0.82[EUR][1000 genomes]
rs17133844	0.89[EUR][1000 genomes]
rs17133848	0.83[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs17133858	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1801906	0.82[EUR][1000 genomes]
rs2035208	0.82[EUR][1000 genomes]
rs34827001	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41298117	1.00[EUR][1000 genomes]
rs41298121	0.82[EUR][1000 genomes]
rs4362167	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56738638	0.82[EUR][1000 genomes]
rs56958854	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57277559	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57279023	0.82[EUR][1000 genomes]
rs57654883	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59940449	0.87[EUR][1000 genomes]
rs60893479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61265142	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67495709	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67947456	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72998568	0.92[EUR][1000 genomes]
rs72998587	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72998590	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72998593	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72998594	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72998602	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73488764	0.82[EUR][1000 genomes]
rs7924924	0.82[EUR][1000 genomes]
rs7927925	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7951787	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049887	chr11:74937977-75040438	Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1036292	chr11:74937977-75059496	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
3	nsv1041640	chr11:74945824-75174688	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	94 gene(s)	inside rSNPs	diseases
4	nsv832211	chr11:74945839-75106125	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
5	esv3338705	chr11:74950304-74954802	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv3357620	chr11:74951054-74954252	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv3416910	chr11:74951204-74954302	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv3322804	chr11:74951829-74954677	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74953400-74956600	Weak transcription	Pancreas	Pancrea
2	chr11:74953400-74957000	Weak transcription	Right Atrium	heart

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