Variant report

Variant	rs611013
Chromosome Location	chr11:58480742-58480743
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:58456720..58459253-chr11:58480409..58482286,2	K562	blood:

Variant related genes	Relation type
ENSG00000197254	Chromatin interaction

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

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

rs_ID	r²[population]
rs10501373	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10896831	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10896846	0.90[AMR][1000 genomes]
rs10896855	0.90[AMR][1000 genomes]
rs11229621	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11229624	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11229647	0.90[AMR][1000 genomes]
rs11229660	0.90[AMR][1000 genomes]
rs11229665	0.90[AMR][1000 genomes]
rs11229669	0.90[AMR][1000 genomes]
rs11229675	0.90[AMR][1000 genomes]
rs12365539	0.90[AMR][1000 genomes]
rs12576002	0.90[AMR][1000 genomes]
rs1893630	0.90[AMR][1000 genomes]
rs1938700	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1938706	0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1938710	0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1938712	0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1938720	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1938721	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1938726	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1938727	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1943275	0.90[AMR][1000 genomes]
rs2212844	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2497369	0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2507835	0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs34745169	0.80[AMR][1000 genomes]
rs4554906	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs494174	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs499891	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs511857	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs520075	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs539085	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs540592	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs542683	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59373194	0.81[AFR][1000 genomes]
rs60207372	0.81[AFR][1000 genomes]
rs608998	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs610165	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs615701	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs625951	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs660503	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs666476	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs675815	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[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	nsv832168	chr11:58394060-58564651	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58476800-58481800	Strong transcription	Adipose Nuclei	Adipose
2	chr11:58476800-58485400	Strong transcription	Liver	Liver
3	chr11:58480000-58493200	Weak transcription	Fetal Kidney	kidney

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