Variant report

Variant	rs858060
Chromosome Location	chr20:24222452-24222453
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs112837	0.97[ASN][1000 genomes]
rs2644845	0.84[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs2644846	0.84[ASN][1000 genomes]
rs2748885	0.84[ASN][1000 genomes]
rs2749425	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2749427	0.83[ASN][1000 genomes]
rs2749459	0.81[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs472526	0.83[ASN][1000 genomes]
rs473253	0.83[ASN][1000 genomes]
rs482337	0.83[ASN][1000 genomes]
rs485747	0.81[ASN][1000 genomes]
rs491653	0.87[CEU][hapmap];0.80[CHB][hapmap];0.92[JPT][hapmap]
rs492884	0.83[ASN][1000 genomes]
rs494639	0.83[ASN][1000 genomes]
rs495354	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs496268	0.80[CHB][hapmap];0.85[JPT][hapmap]
rs501262	0.83[ASN][1000 genomes]
rs502250	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs504500	0.83[ASN][1000 genomes]
rs504964	0.83[ASN][1000 genomes]
rs512615	0.84[ASN][1000 genomes]
rs512754	0.81[ASN][1000 genomes]
rs513654	0.81[ASN][1000 genomes]
rs523233	0.84[ASN][1000 genomes]
rs525009	0.84[ASN][1000 genomes]
rs527873	0.84[ASN][1000 genomes]
rs529070	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs529793	0.84[ASN][1000 genomes]
rs530523	0.84[ASN][1000 genomes]
rs530615	0.84[ASN][1000 genomes]
rs531361	0.83[ASN][1000 genomes]
rs545266	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs546094	0.84[ASN][1000 genomes]
rs546946	0.84[ASN][1000 genomes]
rs547449	0.84[ASN][1000 genomes]
rs550792	0.84[ASN][1000 genomes]
rs562594	0.83[ASN][1000 genomes]
rs563102	0.81[ASN][1000 genomes]
rs564245	0.83[ASN][1000 genomes]
rs564337	0.83[ASN][1000 genomes]
rs565074	0.83[ASN][1000 genomes]
rs565833	0.81[ASN][1000 genomes]
rs566047	0.83[ASN][1000 genomes]
rs566089	0.83[ASN][1000 genomes]
rs569066	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs570480	0.81[ASN][1000 genomes]
rs572702	0.84[ASN][1000 genomes]
rs573964	0.83[ASN][1000 genomes]
rs6049501	0.83[ASN][1000 genomes]
rs6049502	0.83[ASN][1000 genomes]
rs6049503	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6049504	0.83[ASN][1000 genomes]
rs6138237	0.83[ASN][1000 genomes]
rs858061	0.97[ASN][1000 genomes]
rs858066	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs858067	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs858068	0.98[ASN][1000 genomes]
rs858069	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858070	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858071	0.97[ASN][1000 genomes]
rs858072	0.85[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs858074	0.84[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	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv3328348	chr20:24095746-24285830	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv833945	chr20:24163437-24349462	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1058146	chr20:24210196-24531087	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24222400-24222600	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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