Variant report

Variant	rs6574487
Chromosome Location	chr14:79549237-79549238
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10138160	1.00[AFR][1000 genomes]
rs10138639	0.81[ASN][1000 genomes]
rs10139370	0.81[ASN][1000 genomes]
rs10139445	0.81[ASN][1000 genomes]
rs11622043	0.81[ASN][1000 genomes]
rs12893811	0.81[ASN][1000 genomes]
rs1875597	0.81[ASN][1000 genomes]
rs2202173	0.81[ASN][1000 genomes]
rs2202174	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2202176	0.99[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2202177	0.81[ASN][1000 genomes]
rs2202178	0.98[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2202181	0.81[ASN][1000 genomes]
rs2221299	0.81[ASN][1000 genomes]
rs2221300	0.81[ASN][1000 genomes]
rs2653539	0.81[ASN][1000 genomes]
rs4141948	0.97[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4243661	0.81[ASN][1000 genomes]
rs4243662	0.81[ASN][1000 genomes]
rs4542593	0.81[ASN][1000 genomes]
rs4635270	0.81[ASN][1000 genomes]
rs4903826	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4903827	0.94[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4903831	0.81[ASN][1000 genomes]
rs5023075	0.81[ASN][1000 genomes]
rs6574484	0.99[AFR][1000 genomes]
rs6574485	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6574488	0.81[ASN][1000 genomes]
rs6574489	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6574490	0.81[ASN][1000 genomes]
rs7143117	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7144999	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7145587	1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7156110	1.00[AFR][1000 genomes]
rs8005119	0.81[ASN][1000 genomes]
rs8021865	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv948724	chr14:79484233-79614043	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv565247	chr14:79508316-79555651	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv2761846	chr14:79522198-79629157	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79547200-79555800	Weak transcription	Colon Smooth Muscle	Colon
2	chr14:79547800-79556800	Weak transcription	Stomach Smooth Muscle	stomach

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