Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12584722	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36101238	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4351942	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4359326	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4441145	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4592544	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4884962	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4884964	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7328868	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7331635	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7993684	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9527191	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9536678	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9536679	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9536681	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9536682	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9563209	0.89[EUR][1000 genomes]
rs9563210	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9563211	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9563212	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9569014	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9569015	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9569016	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3375545	chr13:54517432-54908108	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1051063	chr13:54777487-54997866	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv541778	chr13:54777487-54997866	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54880000-54892000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:54880000-54929800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr13:54881400-54891400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:54884800-54891400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr13:54885000-54891200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr13:54885200-54891400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr13:54886200-54887800	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr13:54886400-54887400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:54886600-54891200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr13:54887000-54887200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr13:54887000-54887400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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