Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12385866	0.83[ASN][1000 genomes]
rs1417733	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1417734	0.92[ASN][1000 genomes]
rs1417735	0.83[ASN][1000 genomes]
rs1535648	0.97[ASN][1000 genomes]
rs1535649	0.97[ASN][1000 genomes]
rs17181892	0.83[ASN][1000 genomes]
rs1998502	0.85[ASN][1000 genomes]
rs2093689	0.94[ASN][1000 genomes]
rs4619266	0.88[ASN][1000 genomes]
rs61965636	0.87[ASN][1000 genomes]
rs61965639	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7318373	0.83[ASN][1000 genomes]
rs7985588	0.87[ASN][1000 genomes]
rs7994578	0.97[ASN][1000 genomes]
rs9556408	0.85[ASN][1000 genomes]
rs9556409	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9556410	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9561654	0.83[ASN][1000 genomes]
rs9561655	0.83[ASN][1000 genomes]
rs9561656	0.85[ASN][1000 genomes]
rs9561657	0.85[ASN][1000 genomes]
rs9561660	0.87[ASN][1000 genomes]
rs9561661	0.85[ASN][1000 genomes]
rs9561662	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9584244	0.88[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	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv832686	chr13:95206742-95400992	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr13:95326400-95335600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:95327200-95335600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr13:95330400-95335200	Weak transcription	Esophagus	oesophagus
4	chr13:95330600-95335600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr13:95330600-95335600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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