Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10506206	1.00[CEU][hapmap];0.88[CHB][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11181108	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12302029	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12302915	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12303689	0.81[EUR][1000 genomes]
rs12313459	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12812871	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs12813157	1.00[CEU][hapmap];0.87[CHB][hapmap]
rs12822269	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1495776	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34083464	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34361926	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34637635	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35513252	0.82[EUR][1000 genomes]
rs36074014	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61411957	0.97[EUR][1000 genomes]
rs7307151	1.00[CEU][hapmap];0.88[CHB][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7316877	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs74078263	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7959299	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7967199	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7976931	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs921440	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899040	chr12:41905897-42181706	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv832386	chr12:42017259-42189476	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv899043	chr12:42058138-42313665	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv899044	chr12:42058138-42321161	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42103000-42118800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:42112600-42114400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr12:42113400-42114400	Enhancers	H1 Cell Line	embryonic stem cell
4	chr12:42113800-42114400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:42113800-42114400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr12:42113800-42114400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:42113800-42114400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr12:42114000-42114400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr12:42114000-42114600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:42114200-42114600	Enhancers	Brain Germinal Matrix	brain
11	chr12:42114200-42115000	Enhancers	H9 Cell Line	embryonic stem cell

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