Variant report

Variant	rs6131711
Chromosome Location	chr20:15776418-15776419
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10460644	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16996551	0.91[CEU][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1810505	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1997798	0.90[ASN][1000 genomes]
rs2041422	0.87[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2103709	0.91[CEU][hapmap]
rs2109536	0.91[ASN][1000 genomes]
rs2876413	0.88[CEU][hapmap]
rs4292145	0.90[ASN][1000 genomes]
rs6043538	0.84[CEU][hapmap]
rs6105464	0.81[CEU][hapmap]
rs6131708	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6131709	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6131710	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6131712	0.91[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6131714	0.87[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs6131715	0.87[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs6131716	0.87[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs6131717	0.87[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs6131718	0.87[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs6131726	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6135496	0.80[CEU][hapmap]
rs6135498	0.87[CEU][hapmap]
rs6135503	0.88[CEU][hapmap]
rs6135517	0.84[CEU][hapmap];0.88[EUR][1000 genomes]
rs6135524	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6135525	1.00[CEU][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6135526	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6135547	0.82[EUR][1000 genomes]
rs6135550	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6135551	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6135555	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6135556	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6514612	0.88[CEU][hapmap]
rs761262	0.86[CHB][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs763660	0.87[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8118724	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs979530	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv833928	chr20:15619962-15780758	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv519883	chr20:15738086-15817106	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv585643	chr20:15759361-15796051	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv912793	chr20:15760969-15807441	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv833929	chr20:15765372-15977337	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv1847965	chr20:15766727-15807441	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv585644	chr20:15766727-15807441	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15770800-15780000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr20:15773600-15777600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr20:15775000-15776800	Enhancers	Brain Germinal Matrix	brain
4	chr20:15775200-15776800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:15776400-15776800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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