Variant report

Variant	rs4076998
Chromosome Location	chr15:78025420-78025421
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:78021486..78023162-chr15:78023634..78026490,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10851897	0.83[ASN][1000 genomes]
rs11072662	0.90[EUR][1000 genomes]
rs11072663	0.88[EUR][1000 genomes]
rs11072665	0.89[EUR][1000 genomes]
rs11629729	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11631410	0.83[CEU][hapmap];0.82[CHB][hapmap];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11633354	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11636649	0.80[ASN][1000 genomes]
rs11637588	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11856761	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12438542	0.83[ASN][1000 genomes]
rs12903563	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12911718	0.89[EUR][1000 genomes]
rs12915704	0.81[EUR][1000 genomes]
rs28406214	0.90[EUR][1000 genomes]
rs34906247	0.89[EUR][1000 genomes]
rs35028279	0.90[EUR][1000 genomes]
rs35761651	0.90[EUR][1000 genomes]
rs36058724	0.90[EUR][1000 genomes]
rs3935682	0.82[ASN][1000 genomes]
rs3935683	0.82[ASN][1000 genomes]
rs3935684	0.81[ASN][1000 genomes]
rs3935685	0.82[ASN][1000 genomes]
rs3935831	0.83[ASN][1000 genomes]
rs4073356	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4334265	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4360891	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4468571	0.80[ASN][1000 genomes]
rs4477663	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4578613	0.90[EUR][1000 genomes]
rs4595768	0.90[EUR][1000 genomes]
rs4886521	0.90[EUR][1000 genomes]
rs4886898	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs4886899	0.84[EUR][1000 genomes]
rs4886900	0.81[EUR][1000 genomes]
rs4886902	0.86[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4886904	0.83[ASN][1000 genomes]
rs56370262	0.90[EUR][1000 genomes]
rs58813188	0.82[ASN][1000 genomes]
rs58831466	0.83[ASN][1000 genomes]
rs60917280	0.82[ASN][1000 genomes]
rs62007780	0.83[ASN][1000 genomes]
rs62007781	0.83[ASN][1000 genomes]
rs62007784	0.82[ASN][1000 genomes]
rs6495245	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7175083	0.90[EUR][1000 genomes]
rs7176668	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8027520	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8027667	0.93[EUR][1000 genomes];0.95[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	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS 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	15 gene(s)	inside rSNPs	diseases
4	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	nsv833061	chr15:77998374-78121905	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv570150	chr15:78004743-78038124	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv904420	chr15:78025267-78078903	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78013000-78031200	Weak transcription	Fetal Brain Female	brain
2	chr15:78014000-78031000	Weak transcription	Spleen	Spleen
3	chr15:78020800-78030200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr15:78024800-78027000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:78025000-78025600	Weak transcription	Brain Angular Gyrus	brain
6	chr15:78025000-78025600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:78025000-78025800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr15:78025400-78026400	Enhancers	K562	blood
9	chr15:78025400-78027600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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