Variant report

Variant	rs10265134
Chromosome Location	chr7:47746915-47746916
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10227440	0.95[AFR][1000 genomes]
rs10240563	0.95[AFR][1000 genomes]
rs10245141	0.90[AFR][1000 genomes]
rs10253662	0.95[AFR][1000 genomes]
rs10256699	0.95[AFR][1000 genomes]
rs10274400	0.90[AFR][1000 genomes]
rs11764002	0.95[AFR][1000 genomes]
rs11764105	0.95[AFR][1000 genomes]
rs28766091	0.95[AFR][1000 genomes]
rs28795431	0.95[AFR][1000 genomes]
rs28869205	0.95[AFR][1000 genomes]
rs28886403	0.95[AFR][1000 genomes]
rs28893025	0.95[AFR][1000 genomes]
rs66931702	0.95[AFR][1000 genomes]
rs66979603	0.95[AFR][1000 genomes]
rs67344873	0.95[AFR][1000 genomes]
rs67853780	0.85[AFR][1000 genomes]
rs6974376	0.95[AFR][1000 genomes]
rs73107278	0.95[AFR][1000 genomes]
rs7791862	0.90[AFR][1000 genomes]
rs7792137	0.90[AFR][1000 genomes]
rs7792409	0.90[AFR][1000 genomes]
rs7792432	0.90[AFR][1000 genomes]
rs7792551	0.90[AFR][1000 genomes]
rs7792952	0.95[AFR][1000 genomes]
rs7811157	0.90[AFR][1000 genomes]
rs7811821	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv888003	chr7:47694270-47907214	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1024392	chr7:47707023-47758976	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1018608	chr7:47708525-47831535	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1022906	chr7:47709936-47831535	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv1028355	chr7:47715107-47758976	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1015163	chr7:47734913-47832389	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
8	nsv538831	chr7:47734913-47832389	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
9	nsv526963	chr7:47741157-47750051	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47733000-47750000	Weak transcription	Aorta	Aorta
2	chr7:47734000-47748600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:47734600-47748200	Weak transcription	Fetal Stomach	stomach
4	chr7:47742000-47748600	Weak transcription	A549	lung
5	chr7:47745400-47748600	Weak transcription	Fetal Kidney	kidney

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