Variant report

Variant	rs11922647
Chromosome Location	chr3:151059279-151059280
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr3:151058777-151059362	SK-N-SH	brain:	n/a	n/a

Variant related genes	Relation type
P2RY12	TF binding region

Extended variants
information (count: 41 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10935838	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1352887	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1388619	0.85[ASN][1000 genomes]
rs1388622	0.85[ASN][1000 genomes]
rs1388623	0.85[ASN][1000 genomes]
rs1388624	0.85[ASN][1000 genomes]
rs1388626	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1466684	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1491978	0.84[ASN][1000 genomes]
rs1491979	0.85[ASN][1000 genomes]
rs1491980	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1491981	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1873622	0.87[ASN][1000 genomes]
rs2046934	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2172249	0.96[ASN][1000 genomes]
rs2242353	0.81[AFR][1000 genomes]
rs3732762	0.85[ASN][1000 genomes]
rs3821667	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3971191	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3975401	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3975403	0.85[ASN][1000 genomes]
rs3975404	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4146770	0.84[EUR][1000 genomes]
rs4679802	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4680374	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6440731	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6440732	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6763983	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6769397	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6782212	0.87[ASN][1000 genomes]
rs6790748	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6809699	1.00[EUR][1000 genomes]
rs7615865	0.88[ASN][1000 genomes]
rs7621876	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7633362	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9820422	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9877389	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9878459	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460894	chr3:150770614-151095093	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv592045	chr3:150770614-151095093	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv829757	chr3:151044880-151226442	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151045600-151063600	Weak transcription	Brain Angular Gyrus	brain
2	chr3:151050000-151063600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:151057000-151063200	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:151058800-151063600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr3:151059000-151062800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr3:151059000-151062800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:151059200-151061800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr3:151059200-151063400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:151059200-151063600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:151059200-151063800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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