Variant report

Variant	rs356219
Chromosome Location	chr4:90637601-90637602
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10003708	0.97[ASN][1000 genomes]
rs10033209	0.96[CHB][hapmap];0.96[ASN][1000 genomes]
rs1045722	0.96[ASN][1000 genomes]
rs10516844	0.99[ASN][1000 genomes]
rs10516845	0.91[JPT][hapmap]
rs11931074	0.99[ASN][1000 genomes]
rs11944331	0.90[JPT][hapmap]
rs11945223	0.97[ASN][1000 genomes]
rs12640100	0.98[ASN][1000 genomes]
rs12642514	0.95[ASN][1000 genomes]
rs12648141	0.96[ASN][1000 genomes]
rs17016071	0.96[ASN][1000 genomes]
rs2736990	0.82[JPT][hapmap]
rs2737029	0.86[JPT][hapmap]
rs28393675	0.94[ASN][1000 genomes]
rs28412513	0.96[ASN][1000 genomes]
rs28613708	0.95[ASN][1000 genomes]
rs35541731	0.96[ASN][1000 genomes]
rs356165	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs356168	0.82[JPT][hapmap]
rs356200	0.82[JPT][hapmap]
rs356203	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs356204	0.83[JPT][hapmap]
rs356209	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs356215	0.90[AFR][1000 genomes]
rs356220	0.82[AFR][1000 genomes]
rs3756054	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3775422	0.94[ASN][1000 genomes]
rs3775423	0.83[CHB][hapmap];0.86[JPT][hapmap];0.96[ASN][1000 genomes]
rs3775424	0.96[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3775439	0.86[JPT][hapmap]
rs3796661	0.90[JPT][hapmap]
rs3822086	0.96[ASN][1000 genomes]
rs3822090	0.91[JPT][hapmap]
rs3857051	0.97[ASN][1000 genomes]
rs3857052	0.97[ASN][1000 genomes]
rs3857053	0.96[ASN][1000 genomes]
rs3857057	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3857058	0.96[ASN][1000 genomes]
rs3857059	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4088093	0.96[ASN][1000 genomes]
rs4088094	0.96[ASN][1000 genomes]
rs4122861	0.88[ASN][1000 genomes]
rs61032876	0.97[ASN][1000 genomes]
rs6818319	0.96[ASN][1000 genomes]
rs6826785	0.80[ASN][1000 genomes]
rs6834765	0.90[JPT][hapmap]
rs73831461	0.98[ASN][1000 genomes]
rs7436973	0.97[ASN][1000 genomes]
rs7655792	0.97[ASN][1000 genomes]
rs7661330	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7675290	0.96[ASN][1000 genomes]
rs7681312	0.99[ASN][1000 genomes]
rs7681815	0.99[ASN][1000 genomes]
rs7684318	0.96[ASN][1000 genomes]
rs7690873	0.91[JPT][hapmap]
rs8180209	0.96[ASN][1000 genomes]
rs8180214	0.94[ASN][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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

Variant related diseases (count:2)

Disease	PMID	Source
Parkinson's disease	21292315	GWAS catalog
Parkinson's disease	22438815	GWAS catalog

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90630400-90647400	Weak transcription	Fetal Lung	lung
2	chr4:90630400-90647600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:90630600-90640400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:90630600-90647400	Weak transcription	Ovary	ovary
5	chr4:90631400-90638600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:90634200-90642200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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