Variant report

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

rs_ID	r²[population]
rs10135127	0.83[AMR][1000 genomes]
rs10145565	0.84[GIH][hapmap]
rs10146649	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs10151376	0.82[AMR][1000 genomes]
rs10498527	1.00[CHB][hapmap]
rs1105625	1.00[CHB][hapmap]
rs11158780	0.84[AMR][1000 genomes]
rs11158784	1.00[CHB][hapmap]
rs11158785	1.00[CHB][hapmap]
rs11158786	1.00[CHB][hapmap]
rs1275417	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs12881049	0.82[AMR][1000 genomes]
rs12885977	0.83[AMR][1000 genomes]
rs12891103	0.83[AMR][1000 genomes]
rs1629783	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs1710989	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs1710990	1.00[CHB][hapmap]
rs1710993	1.00[CHB][hapmap]
rs1892296	0.85[AMR][1000 genomes]
rs2001355	1.00[CHB][hapmap]
rs2331918	1.00[CHB][hapmap];0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs35538328	0.83[AMR][1000 genomes]
rs4338726	0.84[AMR][1000 genomes]
rs4899280	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[AMR][1000 genomes]
rs61981619	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7141235	1.00[CHB][hapmap]
rs7151797	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8014402	0.90[ASN][1000 genomes]
rs8017103	0.85[AMR][1000 genomes]
rs9323521	1.00[CHB][hapmap]
rs9323524	0.84[GIH][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832823	chr14:69388853-69567638	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs761899	WDR22	Cis_1M	lymphoblastoid	RTeQTL
rs761899	SPTB	cis	cerebellum	SCAN

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69473000-69503600	Weak transcription	Right Atrium	heart
2	chr14:69486000-69503600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:69496600-69501200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr14:69500800-69501200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:69500800-69501400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:69500800-69502400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr14:69501000-69501400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr14:69501000-69501400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr14:69501000-69501400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr14:69501000-69501800	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr14:69501000-69501800	Enhancers	Fetal Muscle Trunk	muscle
12	chr14:69501000-69502000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:69501000-69502200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr14:69501000-69502400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:69501000-69502600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:69501000-69503000	Enhancers	HUVEC	blood vessel
17	chr14:69501000-69506600	Enhancers	Osteobl	bone

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