Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs62278296	0.90[EUR][1000 genomes]
rs62278346	0.97[EUR][1000 genomes]
rs62279582	0.97[EUR][1000 genomes]
rs62279583	0.97[EUR][1000 genomes]
rs62279584	0.97[EUR][1000 genomes]
rs62279589	0.90[EUR][1000 genomes]
rs62279591	0.97[EUR][1000 genomes]
rs62279616	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279623	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279624	1.00[EUR][1000 genomes]
rs62279627	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279629	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279656	0.89[AMR][1000 genomes]
rs62279657	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62281362	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281364	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281365	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281366	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281466	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
2	nsv829774	chr3:161229405-161386919	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2422309	chr3:161242389-161425932	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv877711	chr3:161275848-161486665	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1004255	chr3:161340249-161476537	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv2755105	chr3:161349991-161371789	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161351000-161355200	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:161351400-161355200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr3:161353000-161353400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:161353000-161353600	Enhancers	H9 Cell Line	embryonic stem cell
5	chr3:161353000-161353800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr3:161353000-161353800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:161353200-161353400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:161353200-161353600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr3:161353200-161354600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:161353200-161359200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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