Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10872562	0.86[CHB][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1108314	0.86[CHB][hapmap]
rs11155315	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11155317	0.80[ASN][1000 genomes]
rs12198291	0.80[EUR][1000 genomes]
rs12207002	0.86[CHB][hapmap];0.80[EUR][1000 genomes]
rs12208927	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs12528456	0.86[CHB][hapmap];0.80[ASN][1000 genomes]
rs3924969	0.80[EUR][1000 genomes]
rs3934959	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6570573	0.83[YRI][hapmap]
rs6901659	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs6907410	0.80[ASN][1000 genomes]
rs6913134	0.81[CHB][hapmap]
rs6915784	0.81[ASN][1000 genomes]
rs7766510	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs7769294	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7772565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7776119	0.91[ASN][1000 genomes]
rs9321933	0.81[YRI][hapmap]
rs9373396	0.82[ASN][1000 genomes]
rs9373397	0.81[CHB][hapmap]
rs9376779	0.89[ASN][1000 genomes]
rs9386042	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs9386043	0.81[CHB][hapmap]
rs9390126	0.80[EUR][1000 genomes]
rs9403521	0.86[CHB][hapmap];0.82[ASN][1000 genomes]
rs9403523	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs9496733	0.81[YRI][hapmap]

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	esv2758084	chr6:143916621-144079976	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759476	chr6:143916621-144079976	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1032369	chr6:143925374-144007513	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv604805	chr6:143930404-144005949	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143980800-143994200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:143981800-143994200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:143991400-143994200	Weak transcription	H1 Cell Line	embryonic stem cell

Quick Search: