Variant report

Variant	rs10743541
Chromosome Location	chr12:25268943-25268944
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10437762	1.00[AFR][1000 genomes]
rs10734738	1.00[AFR][1000 genomes]
rs10842487	1.00[AFR][1000 genomes]
rs1683161	1.00[AMR][1000 genomes]
rs1693360	1.00[AFR][1000 genomes]
rs2200403	1.00[AFR][1000 genomes]
rs2352783	1.00[AFR][1000 genomes]
rs4246230	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4246231	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4285970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4405405	1.00[AFR][1000 genomes]
rs4620806	1.00[AMR][1000 genomes]
rs4963855	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4963856	1.00[AFR][1000 genomes]
rs4963858	1.00[AMR][1000 genomes]
rs61762428	1.00[AMR][1000 genomes]
rs61764369	1.00[AMR][1000 genomes]
rs7953781	1.00[AMR][1000 genomes]
rs7965331	1.00[AFR][1000 genomes]
rs7977773	1.00[AFR][1000 genomes]
rs7978490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7979670	1.00[AFR][1000 genomes]
rs859146	1.00[AMR][1000 genomes]
rs859149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs859150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs860881	1.00[AMR][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	nsv469169	chr12:24692383-25357680	Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised 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	34 gene(s)	inside rSNPs	diseases
2	nsv557775	chr12:24692383-25357680	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv932477	chr12:24705151-25346677	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv1067577	chr12:24791283-25346677	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv529514	chr12:24791283-25346677	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv1041218	chr12:24972019-25304356	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv557796	chr12:25266203-25306458	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr12:25251800-25274600	Weak transcription	Pancreas	Pancrea
2	chr12:25263800-25288800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:25268400-25269000	Enhancers	HepG2	liver
4	chr12:25268400-25269200	Enhancers	Liver	Liver
5	chr12:25268600-25269000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:25268600-25269000	Enhancers	Fetal Kidney	kidney
7	chr12:25268600-25269000	Enhancers	GM12878-XiMat	blood
8	chr12:25268600-25269000	Enhancers	NHEK	skin
9	chr12:25268600-25279400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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