Variant report

Variant	rs7820373
Chromosome Location	chr8:62744087-62744088
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:62741831..62744985-chr8:62746789..62749495,5	K562	blood:

Variant related genes	Relation type
ENSG00000254119	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12544982	0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs12545018	0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1948507	0.82[JPT][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1948508	0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2350926	0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs56016636	0.87[EUR][1000 genomes]
rs56125512	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs56235963	0.87[EUR][1000 genomes]
rs56741469	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56830160	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs57344387	0.97[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs58080416	0.81[EUR][1000 genomes]
rs58710029	0.81[EUR][1000 genomes]
rs59120662	0.91[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs60520860	0.81[EUR][1000 genomes]
rs61568322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62507583	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs62507585	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6471975	1.00[CEU][hapmap];0.88[MKK][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs73255147	0.81[EUR][1000 genomes]
rs73255155	0.81[EUR][1000 genomes]
rs73255157	0.81[EUR][1000 genomes]
rs73682603	0.81[EUR][1000 genomes]
rs73685132	0.91[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs73685137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73685139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73685145	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73685148	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73685149	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73685158	0.81[EUR][1000 genomes]
rs73685159	0.81[EUR][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	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv932198	chr8:62336705-62914562	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv2761430	chr8:62517980-62873803	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1015216	chr8:62517980-62873803	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	esv3363755	chr8:62702301-62764282	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv611427	chr8:62733267-62848952	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv831338	chr8:62736394-62913048	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62735400-62745000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:62738800-62745000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:62739400-62750000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr8:62743600-62744200	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr8:62743600-62744400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:62743600-62744600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr8:62743800-62744200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr8:62743800-62744400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:62743800-62744600	Enhancers	Brain Substantia Nigra	brain
10	chr8:62744000-62745000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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