Variant report

Variant	rs1564559
Chromosome Location	chr4:86559339-86559340
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:86559206..86561371-chr4:86567124..86569221,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10003669	0.89[ASN][1000 genomes]
rs11931290	1.00[CHB][hapmap]
rs11937452	0.92[ASN][1000 genomes]
rs11943623	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12502332	0.86[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs13103706	0.88[CHB][hapmap];0.87[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs13106652	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[AFR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13123541	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs13129615	1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs13131183	0.91[ASN][1000 genomes]
rs13149991	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1482089	0.88[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs2062100	0.88[CHB][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs2869361	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4693120	0.86[CHB][hapmap];0.87[CHD][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs4693711	0.82[CHD][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs4693712	0.85[CHB][hapmap];0.87[CHD][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs4693718	0.88[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs4693719	0.88[CHB][hapmap];0.87[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs4693720	0.86[ASN][1000 genomes]
rs6531839	0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs6815397	0.88[CHB][hapmap];0.87[CHD][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs6849280	0.82[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs7664042	0.88[CHB][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs766570	0.86[ASN][1000 genomes]
rs7681100	0.86[ASN][1000 genomes]
rs7681661	0.86[ASN][1000 genomes]
rs7688899	0.88[CHB][hapmap];0.92[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs7694594	0.89[ASN][1000 genomes]
rs979337	0.88[CHB][hapmap]
rs9994722	0.92[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	nsv519588	chr4:85762385-86591202	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription 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	5 gene(s)	inside rSNPs	diseases
5	esv3450999	chr4:86485840-86773745	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv829999	chr4:86500257-86666019	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1564559	TRAP1	trans	cerebellum	SCAN

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86551400-86575200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:86551800-86561200	Weak transcription	Left Ventricle	heart
3	chr4:86551800-86569600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:86556600-86560800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr4:86557600-86561600	Strong transcription	Primary B cells from cord blood	blood
6	chr4:86558600-86559800	Enhancers	HSMMtube	muscle
7	chr4:86558800-86561800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr4:86559000-86560000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:86559000-86560200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr4:86559000-86561000	Enhancers	K562	blood
11	chr4:86559200-86559400	Enhancers	HSMM	muscle

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