Variant report

Variant	rs6992232
Chromosome Location	chr8:66889992-66889993
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:66888349..66890452-chr8:66932812..66934820,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000147570	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1108213	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1108214	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11985554	1.00[ASN][1000 genomes]
rs11985589	0.98[ASN][1000 genomes]
rs11987304	0.87[ASN][1000 genomes]
rs11987611	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11988417	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11988589	1.00[ASN][1000 genomes]
rs11993927	1.00[ASN][1000 genomes]
rs11994927	1.00[ASN][1000 genomes]
rs11995310	0.83[ASN][1000 genomes]
rs11995784	0.85[ASN][1000 genomes]
rs11996481	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11998621	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16932382	0.87[ASN][1000 genomes]
rs2002333	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2002334	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34174890	0.87[ASN][1000 genomes]
rs3901084	0.91[ASN][1000 genomes]
rs4129057	0.91[ASN][1000 genomes]
rs4620273	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs55695598	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs56246853	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56747456	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57683289	1.00[ASN][1000 genomes]
rs57690026	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58489131	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58881093	0.87[ASN][1000 genomes]
rs62506592	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62506593	0.87[ASN][1000 genomes]
rs62506596	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62506636	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62506637	0.83[EUR][1000 genomes]
rs6472234	0.82[ASN][1000 genomes]
rs66644630	0.82[ASN][1000 genomes]
rs67768803	0.87[ASN][1000 genomes]
rs6981019	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6997506	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7001181	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7011264	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7017127	0.88[AMR][1000 genomes]
rs72650541	0.87[ASN][1000 genomes]
rs7841695	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs870077	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1023239	chr8:66775321-66904124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66873800-66890600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr8:66878800-66893600	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr8:66885400-66890000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:66886600-66892600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr8:66886600-66893600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:66887200-66893600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr8:66887400-66893400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr8:66887400-66893600	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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