Variant report

Variant	rs6469792
Chromosome Location	chr8:120008371-120008372
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10091277	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10505348	0.82[TSI][hapmap]
rs10505351	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10955924	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11573829	0.82[TSI][hapmap]
rs11995824	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13254554	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13260214	0.81[EUR][1000 genomes]
rs13264172	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1385500	0.80[ASN][1000 genomes]
rs1485302	0.86[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs1485303	0.86[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs1485305	0.99[ASN][1000 genomes]
rs1485307	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1485310	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1825512	0.88[ASN][1000 genomes]
rs1872422	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1872423	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1905783	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1905784	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2062376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2062377	0.85[EUR][1000 genomes]
rs2220189	0.89[EUR][1000 genomes]
rs28437165	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28621599	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4273881	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4335155	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4403440	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4403441	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4416847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4424291	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4424296	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4495461	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4567065	0.85[EUR][1000 genomes]
rs4587360	0.98[ASN][1000 genomes]
rs4615609	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4618726	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6469795	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6469797	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6993813	0.82[EUR][1000 genomes]
rs7004052	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7010043	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7010267	0.82[TSI][hapmap]
rs7013722	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7813486	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7824837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7842942	0.85[EUR][1000 genomes]
rs9650075	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[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	nsv868916	chr8:119911943-120762250	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758169	chr8:119943309-120275750	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2759639	chr8:119943309-120275750	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv522241	chr8:119995697-120027871	Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120006400-120008400	Enhancers	Fetal Heart	heart
2	chr8:120007000-120013600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:120007200-120008400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:120007200-120008400	Enhancers	NH-A	brain
5	chr8:120007800-120008400	Enhancers	Right Ventricle	heart
6	chr8:120008000-120012400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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