Variant report

Variant	rs1522755
Chromosome Location	chr11:59122623-59122624
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:59119912..59122779-chr11:59129911..59131967,2	K562	blood:

Variant related genes	Relation type
ENSG00000176495	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10437722	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10736693	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10736698	0.90[AMR][1000 genomes]
rs10750913	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10750914	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10750920	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10792229	1.00[EUR][1000 genomes]
rs10896959	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11229909	1.00[EUR][1000 genomes]
rs1357375	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1597989	0.81[AFR][1000 genomes]
rs1608214	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1829806	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1894123	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1949710	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs1977985	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2027773	0.90[AMR][1000 genomes]
rs2097162	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2187530	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2213079	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2213080	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2213082	0.90[AMR][1000 genomes]
rs4438055	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4479010	1.00[AMR][1000 genomes]
rs4494319	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4556553	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56204747	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6591519	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7927986	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7944381	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs940022	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv948365	chr11:58515163-59156405	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	nsv1046084	chr11:59034871-59314519	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv541052	chr11:59119390-59185103	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59122200-59123600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr11:59122400-59123400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:59122400-59123800	Enhancers	Pancreas	Pancrea

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