Variant report

Variant	rs13238777
Chromosome Location	chr7:14496815-14496816
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10247453	0.82[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs10263131	0.81[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1030578	0.82[EUR][1000 genomes]
rs10499441	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs11771951	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12699619	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12699621	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1367780	0.83[EUR][1000 genomes]
rs1431532	0.89[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs1978671	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2116314	0.81[EUR][1000 genomes]
rs2884348	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34919207	0.80[EUR][1000 genomes]
rs4607508	0.92[EUR][1000 genomes]
rs4719405	0.99[EUR][1000 genomes]
rs4719406	0.84[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs4719407	0.83[EUR][1000 genomes]
rs4721335	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs4721336	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs4721337	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs6943928	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7777868	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7782805	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7783911	0.94[EUR][1000 genomes]
rs7793372	0.80[EUR][1000 genomes]
rs7794554	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9690425	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	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	chr7:14496600-14497200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr7:14496600-14497600	Enhancers	Fetal Heart	heart

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