Variant report

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

rs_ID	r²[population]
rs10942721	0.83[ASN][1000 genomes]
rs10942722	0.83[ASN][1000 genomes]
rs10942723	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11739370	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs11740894	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11745011	0.88[ASN][1000 genomes]
rs11745016	0.88[ASN][1000 genomes]
rs11745686	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11746386	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1455786	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55979253	0.88[ASN][1000 genomes]
rs56831970	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58925145	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62367818	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6453091	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6894292	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7700681	0.89[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs7719022	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7721009	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7722489	0.84[CHB][hapmap];0.90[JPT][hapmap]

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	nsv518286	chr5:74169045-74243120	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830352	chr5:74189495-74337944	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74192000-74199000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:74197400-74199000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:74197600-74198600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:74197600-74198800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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