Variant report

Variant	rs6513754
Chromosome Location	chr20:40597076-40597077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:40596592..40599038-chr20:40600387..40603360,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs2223912	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2866988	1.00[EUR][1000 genomes]
rs3084007	0.89[EUR][1000 genomes]
rs41278136	0.83[EUR][1000 genomes]
rs41278142	0.83[EUR][1000 genomes]
rs58841508	0.83[EUR][1000 genomes]
rs6016670	0.89[EUR][1000 genomes]
rs6016681	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6016682	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6029966	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6093550	0.82[EUR][1000 genomes]
rs6093551	0.80[EUR][1000 genomes]
rs6102616	1.00[EUR][1000 genomes]
rs6102641	0.87[EUR][1000 genomes]
rs6513765	0.83[EUR][1000 genomes]
rs73113854	0.98[EUR][1000 genomes]
rs73113856	0.98[EUR][1000 genomes]
rs73113859	0.98[EUR][1000 genomes]
rs73113864	0.98[EUR][1000 genomes]
rs73113865	0.98[EUR][1000 genomes]
rs73113870	0.91[EUR][1000 genomes]
rs73113872	0.89[EUR][1000 genomes]
rs73115457	0.89[EUR][1000 genomes]
rs73115458	0.89[EUR][1000 genomes]
rs73115478	0.89[EUR][1000 genomes]
rs73115479	0.89[EUR][1000 genomes]
rs73115480	0.89[EUR][1000 genomes]
rs73117860	0.85[EUR][1000 genomes]
rs73117872	0.89[EUR][1000 genomes]
rs73117886	0.85[EUR][1000 genomes]
rs73119803	0.83[EUR][1000 genomes]
rs73119807	0.83[EUR][1000 genomes]
rs73119815	0.83[EUR][1000 genomes]
rs73119820	0.83[EUR][1000 genomes]
rs73119823	0.83[EUR][1000 genomes]
rs73119847	0.83[EUR][1000 genomes]
rs73119850	0.83[EUR][1000 genomes]
rs73122781	0.93[EUR][1000 genomes]
rs73122800	1.00[EUR][1000 genomes]
rs73124713	1.00[EUR][1000 genomes]
rs73124714	1.00[EUR][1000 genomes]
rs73124722	1.00[EUR][1000 genomes]
rs73124730	1.00[EUR][1000 genomes]
rs73129112	0.83[EUR][1000 genomes]
rs73129138	0.83[EUR][1000 genomes]
rs73129147	0.83[EUR][1000 genomes]
rs73129161	0.83[EUR][1000 genomes]
rs73129169	0.83[EUR][1000 genomes]
rs73129170	0.83[EUR][1000 genomes]
rs73129176	0.83[EUR][1000 genomes]
rs73129180	0.83[EUR][1000 genomes]
rs73129186	0.83[EUR][1000 genomes]
rs8120362	1.00[EUR][1000 genomes]
rs8124637	0.83[EUR][1000 genomes]

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	nsv3381	chr20:39925326-40765696	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv833986	chr20:40468902-40628365	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:40597000-40599600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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