Variant report

Variant	rs73085831
Chromosome Location	chr4:8337375-8337376
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:8321399..8323453-chr4:8336725..8338364,2	K562	blood:
2	chr4:8337029..8339751-chr4:8340402..8342759,2	K562	blood:
3	chr4:8315694..8318647-chr4:8336893..8339393,2	K562	blood:

Variant related genes	Relation type
ENSG00000249145	Chromatin interaction
ENSG00000248986	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1111639	1.00[ASN][1000 genomes]
rs1720009	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2619302	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28464380	1.00[EUR][1000 genomes]
rs28494604	1.00[EUR][1000 genomes]
rs28527236	1.00[EUR][1000 genomes]
rs28545268	1.00[EUR][1000 genomes]
rs34061748	1.00[EUR][1000 genomes]
rs58156849	1.00[EUR][1000 genomes]
rs58480457	1.00[ASN][1000 genomes]
rs61020869	1.00[EUR][1000 genomes]
rs73083700	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73085819	1.00[EUR][1000 genomes]
rs73085820	1.00[EUR][1000 genomes]
rs73085829	1.00[ASN][1000 genomes]
rs73085836	1.00[EUR][1000 genomes]
rs73799117	1.00[EUR][1000 genomes]
rs73799119	1.00[EUR][1000 genomes]
rs73799140	1.00[ASN][1000 genomes]
rs7673493	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9986093	1.00[ASN][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	nsv1002794	chr4:8110083-8490934	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv878595	chr4:8154534-8390646	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv878601	chr4:8214767-8440951	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv878602	chr4:8214767-8448992	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1009011	chr4:8225669-8424831	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv470013	chr4:8315938-8377058	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv878605	chr4:8332057-8378959	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8325600-8338400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:8333400-8342400	Weak transcription	Psoas Muscle	Psoas
3	chr4:8333400-8342400	Weak transcription	Right Atrium	heart
4	chr4:8334800-8337800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:8335000-8337600	Weak transcription	HMEC	breast
6	chr4:8335000-8338000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:8335000-8338400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:8336600-8337400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:8336600-8337400	Enhancers	Pancreas	Pancrea
10	chr4:8336800-8337400	Enhancers	Right Ventricle	heart
11	chr4:8337200-8337400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:8337200-8337600	Enhancers	HepG2	liver
13	chr4:8337200-8341800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr4:8337200-8342400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:8337200-8343200	Weak transcription	Fetal Kidney	kidney

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