Variant report

Variant	rs7587816
Chromosome Location	chr2:209474656-209474657
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs10205752	0.90[EUR][1000 genomes]
rs11899150	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11899194	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12473851	0.92[EUR][1000 genomes]
rs12477234	0.92[EUR][1000 genomes]
rs12477763	0.94[EUR][1000 genomes]
rs12694117	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13398234	0.91[EUR][1000 genomes]
rs1429879	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17664172	0.90[EUR][1000 genomes]
rs1835300	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1835301	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1921738	0.91[EUR][1000 genomes]
rs1921739	0.91[EUR][1000 genomes]
rs2115772	0.90[EUR][1000 genomes]
rs2115773	0.90[EUR][1000 genomes]
rs2364138	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4675783	0.81[ASN][1000 genomes]
rs58160491	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61496025	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62193738	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62193740	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62193742	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62193757	0.82[EUR][1000 genomes]
rs6435469	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6435470	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6704637	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7561452	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7566150	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7592555	0.92[EUR][1000 genomes]
rs7605516	0.84[AMR][1000 genomes];0.99[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	nsv1005292	chr2:209470753-209631662	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv2756959	chr2:209472551-209551952	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2759112	chr2:209472551-209551952	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv875753	chr2:209474223-209517915	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7587816	KLF7	cis	parietal	SCAN
rs7587816	CPO	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209474400-209479600	Weak transcription	K562	blood
2	chr2:209474400-209480200	Weak transcription	Fetal Heart	heart

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