Variant report

Variant	rs10820928
Chromosome Location	chr9:94726750-94726751
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94724723..94727442-chr9:94727772..94730585,2	K562	blood:
2	chr9:94725749..94728020-chr9:94875942..94878180,2	MCF-7	breast:
3	chr9:94725942..94727909-chr9:94729085..94731024,2	K562	blood:

Variant related genes	Relation type
ENSG00000090054	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10820916	0.91[EUR][1000 genomes]
rs10820921	0.95[CEU][hapmap];0.93[EUR][1000 genomes]
rs10820922	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10820925	0.82[ASN][1000 genomes]
rs10820933	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10820934	0.90[CEU][hapmap];0.85[CHB][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10820939	0.86[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes]
rs10992161	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs10992166	0.93[EUR][1000 genomes]
rs10992168	0.92[EUR][1000 genomes]
rs10992172	0.82[ASN][1000 genomes]
rs10992196	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10992208	0.87[AMR][1000 genomes]
rs10992218	0.86[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes]
rs10992219	0.86[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes]
rs10992224	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes]
rs10992250	0.82[JPT][hapmap]
rs11790093	0.87[AMR][1000 genomes]
rs11790991	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes]
rs12377635	0.86[AMR][1000 genomes]
rs12380093	0.86[AMR][1000 genomes]
rs12554679	0.91[CEU][hapmap]
rs1534534	0.86[CEU][hapmap]
rs17749165	1.00[CHB][hapmap]
rs1892263	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1919101	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3932420	0.93[EUR][1000 genomes]
rs55939422	0.86[AMR][1000 genomes]
rs56013831	0.92[EUR][1000 genomes]
rs56217921	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56272949	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56280154	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56309039	0.92[EUR][1000 genomes]
rs62565755	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62567925	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62567926	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62567930	0.86[AMR][1000 genomes]
rs62567931	0.86[AMR][1000 genomes]
rs7034006	0.86[CEU][hapmap];1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs7038397	0.82[CEU][hapmap];0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs7038823	0.86[CEU][hapmap]
rs72746290	0.82[ASN][1000 genomes]
rs72746299	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7857759	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes]
rs7871522	0.86[CEU][hapmap];1.00[CHB][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv1046733	chr9:94690622-95138564	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv831653	chr9:94692454-94867542	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv530947	chr9:94697309-95093377	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94726000-94726800	Enhancers	HMEC	breast
2	chr9:94726400-94734800	Weak transcription	Right Atrium	heart
3	chr9:94726600-94728400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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