Variant report

Variant	rs7957105
Chromosome Location	chr12:63686663-63686664
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10219539	1.00[AMR][1000 genomes]
rs10437962	0.90[AFR][1000 genomes]
rs1107023	0.90[AFR][1000 genomes]
rs11174929	0.88[AFR][1000 genomes]
rs11174945	0.90[AFR][1000 genomes]
rs11174959	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1143806	1.00[AMR][1000 genomes]
rs12299909	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12300351	1.00[AMR][1000 genomes]
rs12309887	0.88[AFR][1000 genomes]
rs12311676	1.00[AMR][1000 genomes]
rs12318068	0.81[AFR][1000 genomes]
rs12322829	1.00[AMR][1000 genomes]
rs3929414	0.88[AFR][1000 genomes]
rs699625	1.00[AMR][1000 genomes]
rs7315546	1.00[AMR][1000 genomes]
rs74097349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7979930	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046836	chr12:63392391-64377169	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv1035736	chr12:63526274-63920372	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541510	chr12:63526274-63920372	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1052866	chr12:63562442-63879794	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv541511	chr12:63562442-63879794	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv832438	chr12:63571652-63745827	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 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	chr12:63680000-63689600	Enhancers	Dnd41	blood
2	chr12:63684400-63689400	Enhancers	Fetal Kidney	kidney
3	chr12:63686200-63688400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:63686200-63688800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:63686200-63689000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:63686400-63687000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:63686600-63686800	Enhancers	Fetal Stomach	stomach
8	chr12:63686600-63687600	Enhancers	A549	lung
9	chr12:63686600-63688200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:63686600-63688800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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