Variant report

Variant	rs2204681
Chromosome Location	chr12:40962147-40962148
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10431578	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10506171	0.82[ASN][1000 genomes]
rs11177109	0.84[JPT][hapmap]
rs11177169	0.82[ASN][1000 genomes]
rs11177179	0.86[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs11177184	0.82[ASN][1000 genomes]
rs11177260	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs11177334	0.82[ASN][1000 genomes]
rs11177345	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11177352	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11177354	0.81[ASN][1000 genomes]
rs11561483	0.82[ASN][1000 genomes]
rs11832449	0.86[CHB][hapmap];0.84[JPT][hapmap];0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs11838212	0.86[CHB][hapmap];0.84[JPT][hapmap];0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12227829	0.82[ASN][1000 genomes]
rs12230855	0.86[ASN][1000 genomes]
rs12230872	0.82[ASN][1000 genomes]
rs12231820	0.82[ASN][1000 genomes]
rs1463738	0.86[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs1492315	0.82[ASN][1000 genomes]
rs1918946	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1918947	0.82[ASN][1000 genomes]
rs1918949	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1965309	0.82[ASN][1000 genomes]
rs2201174	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3751167	0.82[ASN][1000 genomes]
rs3751168	0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs3751175	0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs3829294	0.86[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs3920440	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4768294	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5002282	0.87[CHB][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs58355196	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66485183	0.82[ASN][1000 genomes]
rs66518640	0.82[ASN][1000 genomes]
rs7133098	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs7134929	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7299467	0.82[ASN][1000 genomes]
rs7304329	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs7308403	0.82[ASN][1000 genomes]
rs7308996	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7310318	0.82[ASN][1000 genomes]
rs73269994	0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs73271812	0.82[ASN][1000 genomes]
rs7979493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8181694	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv832378	chr12:40943111-41132305	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv683	chr12:40951473-40996258	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40947400-40967800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:40956000-40963600	Weak transcription	GM12878-XiMat	blood
3	chr12:40961400-40962200	Weak transcription	A549	lung

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