Variant report

Variant	rs8003822
Chromosome Location	chr14:42093431-42093432
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10131184	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs10140527	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs10483526	0.95[EUR][1000 genomes]
rs1111177	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1111179	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11157240	0.81[EUR][1000 genomes]
rs11157241	0.84[EUR][1000 genomes]
rs11157242	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs1117723	0.82[CHB][hapmap];0.83[CHD][hapmap];0.89[JPT][hapmap]
rs1137567	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs12100476	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs12100840	0.88[CHB][hapmap];0.89[JPT][hapmap]
rs12100891	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs12431444	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12589043	0.81[AMR][1000 genomes]
rs12589180	0.82[ASN][1000 genomes]
rs12590527	0.82[ASN][1000 genomes]
rs1609735	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17112133	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs17112137	0.80[ASN][1000 genomes]
rs17112148	0.83[ASN][1000 genomes]
rs17781288	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs1950831	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1950834	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1950835	0.96[CEU][hapmap];0.94[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1950836	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1950838	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1956446	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs1956447	0.89[JPT][hapmap]
rs1956450	0.95[EUR][1000 genomes]
rs1983711	0.80[EUR][1000 genomes]
rs1998126	0.80[ASN][1000 genomes]
rs2121708	0.89[EUR][1000 genomes]
rs2166751	0.88[ASN][1000 genomes]
rs28755010	0.81[ASN][1000 genomes]
rs2899928	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs4356390	0.90[EUR][1000 genomes]
rs59063354	0.83[ASN][1000 genomes]
rs59937937	0.82[ASN][1000 genomes]
rs61990286	0.91[EUR][1000 genomes]
rs61990288	0.91[EUR][1000 genomes]
rs61990289	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6572097	0.81[CHB][hapmap];0.85[CHD][hapmap];0.89[JPT][hapmap]
rs6572099	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7148091	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72684563	0.97[EUR][1000 genomes]
rs8007172	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8013655	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[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	nsv1047300	chr14:41671653-42361098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv1831164	chr14:41673017-42103168	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv533968	chr14:41882101-42327882	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1042078	chr14:41993985-42120143	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2758353	chr14:42045873-42259511	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2759983	chr14:42045873-42259511	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8003822	LRFN5	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42093200-42094200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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