Variant report

Variant	rs11996481
Chromosome Location	chr8:66896532-66896533
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:66894580..66896752-chr8:66901785..66904644,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1108213	0.87[AMR][1000 genomes]
rs1108214	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11985554	0.93[ASN][1000 genomes]
rs11985589	0.91[ASN][1000 genomes]
rs11987304	0.80[ASN][1000 genomes]
rs11987611	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11988417	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11988589	0.93[ASN][1000 genomes]
rs11993927	0.93[ASN][1000 genomes]
rs11994927	0.93[ASN][1000 genomes]
rs11998621	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16932382	0.80[ASN][1000 genomes]
rs2002333	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2002334	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34174890	0.80[ASN][1000 genomes]
rs3901084	0.84[ASN][1000 genomes]
rs4129057	0.84[ASN][1000 genomes]
rs4620273	0.80[ASN][1000 genomes]
rs56246853	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56747456	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57683289	0.93[ASN][1000 genomes]
rs57690026	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58489131	0.86[AMR][1000 genomes]
rs58881093	0.80[ASN][1000 genomes]
rs62506592	0.80[ASN][1000 genomes]
rs62506593	0.80[ASN][1000 genomes]
rs62506596	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62506636	0.89[AMR][1000 genomes]
rs67768803	0.80[ASN][1000 genomes]
rs6981019	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6992232	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6997506	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7001181	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7011264	0.89[AMR][1000 genomes]
rs7017127	0.85[AMR][1000 genomes]
rs72650541	0.80[ASN][1000 genomes]
rs7841695	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs870077	0.80[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:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66890600-66896800	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:66892000-66896800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:66893800-66901800	Weak transcription	Spleen	Spleen
4	chr8:66894000-66897600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:66894800-66904000	Weak transcription	Primary T cells from cord blood	blood
6	chr8:66894800-66904400	Weak transcription	Thymus	Thymus
7	chr8:66895000-66904400	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr8:66895200-66900200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr8:66895400-66896600	ZNF genes & repeats	GM12878-XiMat	blood

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