Variant report

Variant	rs12302239
Chromosome Location	chr12:62832894-62832895
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:62831694..62834470-chr12:62994820..62998671,4	MCF-7	breast:
2	chr12:62826484..62828311-chr12:62831647..62833502,2	K562	blood:

Variant related genes	Relation type
ENSG00000257354	Chromatin interaction
ENSG00000221949	Chromatin interaction
ENSG00000199179	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10160955	0.89[CHB][hapmap]
rs10506440	0.89[CHB][hapmap]
rs10784292	0.88[CHB][hapmap]
rs10877820	0.89[CHB][hapmap]
rs10877826	0.86[CHB][hapmap]
rs10877834	0.89[CHB][hapmap]
rs11174399	0.85[CHB][hapmap]
rs11174436	0.89[CHB][hapmap]
rs11174446	0.88[CEU][hapmap];0.89[CHB][hapmap]
rs11174458	0.89[CHB][hapmap]
rs11174543	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs11836268	0.89[CHB][hapmap]
rs12297474	0.89[CHB][hapmap]
rs12308140	0.89[CHB][hapmap];0.90[JPT][hapmap]
rs12308455	0.89[CHB][hapmap]
rs12310651	0.89[CHB][hapmap]
rs12311279	0.86[CHB][hapmap]
rs12318287	0.88[CHB][hapmap]
rs2167287	0.89[CHB][hapmap]
rs3803106	0.89[CHB][hapmap]
rs7295013	0.82[CHB][hapmap]
rs7300928	0.89[CHB][hapmap]
rs7308473	0.80[AFR][1000 genomes]
rs7309209	0.89[CHB][hapmap]
rs7963950	0.89[CHB][hapmap]
rs9634284	0.89[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530690	chr12:62678463-62999462	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv899157	chr12:62783967-62843620	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv899158	chr12:62783967-62937259	Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv899159	chr12:62783967-62945245	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv821671	chr12:62794304-63007964	Strong transcription ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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