Variant report

Variant	rs11072672
Chromosome Location	chr15:78069844-78069845
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11072677	0.83[ASN][1000 genomes]
rs11072678	0.93[EUR][1000 genomes]
rs11852404	0.94[ASN][1000 genomes]
rs11852704	0.83[ASN][1000 genomes]
rs11855944	0.94[ASN][1000 genomes]
rs11857499	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11857839	0.90[ASN][1000 genomes]
rs11857968	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11858003	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12441624	0.94[ASN][1000 genomes]
rs12441953	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12906902	0.94[ASN][1000 genomes]
rs12911998	0.82[AMR][1000 genomes]
rs12912051	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12914963	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34000202	0.94[ASN][1000 genomes]
rs35265558	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35487286	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35840713	0.84[EUR][1000 genomes]
rs35977825	0.84[EUR][1000 genomes]
rs36055448	0.84[ASN][1000 genomes]
rs4075024	0.90[ASN][1000 genomes]
rs4075981	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4304989	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4886913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4886916	0.94[ASN][1000 genomes]
rs4886923	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4886925	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4886940	0.83[EUR][1000 genomes]
rs4886945	0.83[EUR][1000 genomes]
rs56061966	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58455314	0.82[AFR][1000 genomes]
rs60777884	0.81[AFR][1000 genomes]
rs61085022	0.81[AFR][1000 genomes]
rs7164311	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7170767	0.94[ASN][1000 genomes]
rs7175762	0.94[ASN][1000 genomes]
rs7175927	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7181312	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7182069	0.94[ASN][1000 genomes]
rs72730744	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72730767	0.83[EUR][1000 genomes]
rs72730772	0.83[EUR][1000 genomes]
rs72730774	0.83[EUR][1000 genomes]
rs72730775	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 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	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
4	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
5	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
6	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
7	nsv833062	chr15:78035206-78220358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv904421	chr15:78041789-78129964	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv904422	chr15:78055479-78106177	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv904423	chr15:78059488-78119345	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv904424	chr15:78059488-78158893	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv471255	chr15:78063585-78131097	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv570171	chr15:78064664-78131097	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv904425	chr15:78064664-78153850	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv3513853	chr15:78064897-78069995	Weak transcription Enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78061800-78074800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:78066600-78072600	Weak transcription	Fetal Intestine Small	intestine
3	chr15:78068000-78073000	Weak transcription	Fetal Brain Female	brain
4	chr15:78068000-78076400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr15:78068200-78078200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr15:78069200-78072200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr15:78069600-78070400	Weak transcription	Spleen	Spleen
8	chr15:78069800-78072000	Weak transcription	Fetal Brain Male	brain

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