Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1028976	0.90[ASN][1000 genomes]
rs1397780	0.90[ASN][1000 genomes]
rs1511317	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1698242	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1698245	0.84[AFR][1000 genomes]
rs1698265	0.90[ASN][1000 genomes]
rs1698269	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1705632	0.90[ASN][1000 genomes]
rs1705634	0.89[ASN][1000 genomes]
rs1705635	0.89[ASN][1000 genomes]
rs1705654	0.95[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1705656	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1705657	0.89[ASN][1000 genomes]
rs1756281	0.87[AFR][1000 genomes]
rs1756286	0.80[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1756288	0.88[ASN][1000 genomes]
rs7147248	0.88[ASN][1000 genomes]
rs7148616	0.89[ASN][1000 genomes]
rs8003756	0.88[ASN][1000 genomes]
rs8003896	0.85[ASN][1000 genomes]
rs951065	0.90[ASN][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	esv2751287	chr14:84294487-84338247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv565375	chr14:84299666-84336944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1054166	chr14:84299761-84338200	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1036610	chr14:84299761-84338626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1051093	chr14:84303380-84338626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv431019	chr14:84303525-84365447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84308200-84309000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr14:84308200-84309000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:84308400-84309000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr14:84308800-84309200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:84308800-84309200	Enhancers	Brain Germinal Matrix	brain
6	chr14:84308800-84309200	Enhancers	Fetal Brain Female	brain

Quick Search: