Variant report

Variant	rs12308643
Chromosome Location	chr12:66982526-66982527
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10506486	0.81[ASN][1000 genomes]
rs10878456	0.85[ASN][1000 genomes]
rs10878457	0.86[ASN][1000 genomes]
rs11176275	0.84[ASN][1000 genomes]
rs11176281	0.86[ASN][1000 genomes]
rs11176285	0.86[ASN][1000 genomes]
rs11176286	0.86[ASN][1000 genomes]
rs11176287	0.86[ASN][1000 genomes]
rs11176288	0.86[ASN][1000 genomes]
rs11176289	0.86[ASN][1000 genomes]
rs11176290	0.85[ASN][1000 genomes]
rs11176291	0.85[ASN][1000 genomes]
rs11176292	0.86[ASN][1000 genomes]
rs11176293	0.86[ASN][1000 genomes]
rs11176294	0.86[ASN][1000 genomes]
rs11611371	0.81[ASN][1000 genomes]
rs11614253	0.81[ASN][1000 genomes]
rs12314237	0.86[ASN][1000 genomes]
rs12317142	0.84[ASN][1000 genomes]
rs12424156	0.86[ASN][1000 genomes]
rs12424353	0.84[ASN][1000 genomes]
rs12424354	0.84[ASN][1000 genomes]
rs12424519	0.86[ASN][1000 genomes]
rs12424551	0.81[ASN][1000 genomes]
rs12425766	0.84[ASN][1000 genomes]
rs12426601	0.84[ASN][1000 genomes]
rs12426683	0.84[ASN][1000 genomes]
rs12581890	0.84[ASN][1000 genomes]
rs12812897	0.81[ASN][1000 genomes]
rs12819058	0.84[ASN][1000 genomes]
rs12819736	0.86[ASN][1000 genomes]
rs12833815	0.82[ASN][1000 genomes]
rs1493491	0.81[ASN][1000 genomes]
rs1493492	0.81[ASN][1000 genomes]
rs17181501	0.84[ASN][1000 genomes]
rs17181508	0.84[ASN][1000 genomes]
rs17181587	0.83[ASN][1000 genomes]
rs17779336	0.82[ASN][1000 genomes]
rs17779342	0.84[ASN][1000 genomes]
rs17779375	0.86[ASN][1000 genomes]
rs2870852	0.84[ASN][1000 genomes]
rs2870853	0.84[ASN][1000 genomes]
rs2870854	0.84[ASN][1000 genomes]
rs2870855	0.86[ASN][1000 genomes]
rs2870856	0.86[ASN][1000 genomes]
rs34013266	0.83[ASN][1000 genomes]
rs34274845	0.84[ASN][1000 genomes]
rs34491645	0.84[ASN][1000 genomes]
rs34827947	0.84[ASN][1000 genomes]
rs35544210	0.84[ASN][1000 genomes]
rs35714476	0.83[ASN][1000 genomes]
rs35881203	0.84[ASN][1000 genomes]
rs55921723	0.84[ASN][1000 genomes]
rs55952241	0.84[ASN][1000 genomes]
rs57694406	0.86[ASN][1000 genomes]
rs7134983	0.84[ASN][1000 genomes]
rs7135418	0.84[ASN][1000 genomes]
rs7135606	0.84[ASN][1000 genomes]
rs7137153	0.84[ASN][1000 genomes]
rs71452320	0.82[ASN][1000 genomes]
rs7306716	0.84[ASN][1000 genomes]
rs73323178	0.86[ASN][1000 genomes]
rs73323181	0.86[ASN][1000 genomes]
rs7966602	0.81[ASN][1000 genomes]
rs7968255	0.84[ASN][1000 genomes]
rs7968344	0.84[ASN][1000 genomes]
rs7970748	0.81[ASN][1000 genomes]
rs9706163	0.81[ASN][1000 genomes]
rs987688	0.84[ASN][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	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv832447	chr12:66785814-66990029	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv832449	chr12:66885819-67069953	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3325978	chr12:66920993-67016708	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66978800-66983400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr12:66980000-66983200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:66981000-66982600	Enhancers	GM12878-XiMat	blood
4	chr12:66981200-66993000	Weak transcription	Fetal Brain Female	brain
5	chr12:66982400-66988400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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