Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1147921	1.00[ASN][1000 genomes]
rs1147930	0.99[EUR][1000 genomes]
rs1147931	0.99[EUR][1000 genomes]
rs1147935	0.89[ASN][1000 genomes]
rs1253928	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1253929	1.00[ASN][1000 genomes]
rs1253930	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1253932	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1253933	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1253941	1.00[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1253942	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1253945	0.95[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1628283	0.95[ASN][1000 genomes]
rs1761316	0.95[ASN][1000 genomes]
rs1761331	0.96[ASN][1000 genomes]
rs1779343	0.98[ASN][1000 genomes]
rs1892035	0.98[ASN][1000 genomes]
rs1892037	0.90[ASN][1000 genomes]
rs2799712	0.98[ASN][1000 genomes]
rs750011	0.99[EUR][1000 genomes]
rs915082	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895101	chr10:44909081-45007131	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv550701	chr10:44913113-44935055	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44907000-44918400	Weak transcription	Right Atrium	heart
2	chr10:44912200-44919800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:44913000-44918400	Weak transcription	Fetal Lung	lung
4	chr10:44915800-44919600	Weak transcription	Pancreas	Pancrea
5	chr10:44916400-44919000	Enhancers	Fetal Muscle Leg	muscle
6	chr10:44917200-44918600	Enhancers	Fetal Muscle Trunk	muscle

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