Variant report

Variant	rs10820922
Chromosome Location	chr9:94697364-94697365
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94696439..94698046-chr9:94704884..94707640,2	K562	blood:
2	chr3:179280666..179282550-chr9:94696148..94698847,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136518	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10125466	0.82[CEU][hapmap]
rs10820916	0.93[EUR][1000 genomes]
rs10820921	0.95[CEU][hapmap];0.81[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs10820925	1.00[ASN][1000 genomes]
rs10820928	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10820933	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes]
rs10820934	0.90[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs10820939	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs10992161	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10992165	0.81[EUR][1000 genomes]
rs10992166	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10992168	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10992172	1.00[ASN][1000 genomes]
rs10992196	0.81[AMR][1000 genomes]
rs10992208	0.86[AMR][1000 genomes]
rs10992218	0.86[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes]
rs10992219	0.85[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes]
rs10992224	0.85[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes]
rs11790093	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11790991	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12377635	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12380093	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12554679	0.90[CEU][hapmap]
rs1534534	0.86[CEU][hapmap]
rs17749165	1.00[CHB][hapmap]
rs1892263	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1919101	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3932420	0.96[EUR][1000 genomes]
rs55939422	0.84[AMR][1000 genomes]
rs56013831	0.94[EUR][1000 genomes]
rs56217921	0.84[AMR][1000 genomes]
rs56272949	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56280154	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56309039	0.94[EUR][1000 genomes]
rs62565755	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62567925	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62567926	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs62567930	0.84[AMR][1000 genomes]
rs62567931	0.84[AMR][1000 genomes]
rs6479386	0.82[CEU][hapmap]
rs7034006	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7038397	0.82[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7038823	0.86[CEU][hapmap]
rs72746290	1.00[ASN][1000 genomes]
rs72746299	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7857759	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs7871522	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv530946	chr9:94633154-94715023	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94693200-94697400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:94695600-94697400	Active TSS	Stomach Smooth Muscle	stomach
3	chr9:94695800-94702400	Enhancers	Fetal Lung	lung
4	chr9:94696200-94697400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr9:94696200-94698800	Enhancers	K562	blood
6	chr9:94696400-94697400	Weak transcription	Ovary	ovary
7	chr9:94696600-94697400	Weak transcription	Fetal Stomach	stomach
8	chr9:94697000-94698800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr9:94697200-94697800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:94697200-94698000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:94697200-94698200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:94697200-94698200	Enhancers	Colon Smooth Muscle	Colon
13	chr9:94697200-94700000	Enhancers	Rectal Smooth Muscle	rectum
14	chr9:94697200-94700400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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