Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11621377	0.89[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs11848321	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12884774	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1351384	0.87[ASN][1000 genomes]
rs1351385	0.87[ASN][1000 genomes]
rs1480414	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1480415	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1480416	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17094413	0.89[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs17120591	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17120599	0.86[ASN][1000 genomes]
rs1756583	0.82[ASN][1000 genomes]
rs1958800	0.83[ASN][1000 genomes]
rs4904216	0.86[ASN][1000 genomes]
rs61981249	0.87[ASN][1000 genomes]
rs61981250	0.84[ASN][1000 genomes]
rs61981252	0.86[ASN][1000 genomes]
rs856635	0.87[ASN][1000 genomes]
rs856638	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs856703	0.83[ASN][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	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1048026	chr14:85330544-85686322	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3401331	chr14:85332747-85716351	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv565423	chr14:85427846-85638746	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region 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	chr14:85435200-85435800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:85435200-85436200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:85435400-85436000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:85435600-85436600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr14:85435600-85436600	Enhancers	HMEC	breast

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