Variant report

Variant	rs12540503
Chromosome Location	chr7:52785508-52785509
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10214958	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10215086	0.91[AFR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11238229	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11238230	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11974892	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11980050	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12668035	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1528997	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1528998	0.85[ASN][1000 genomes]
rs1528999	0.92[ASN][1000 genomes]
rs1627324	0.84[ASN][1000 genomes]
rs1649716	0.90[ASN][1000 genomes]
rs1649721	0.87[ASN][1000 genomes]
rs1649727	0.87[ASN][1000 genomes]
rs1649733	0.86[ASN][1000 genomes]
rs1729831	0.84[ASN][1000 genomes]
rs1729857	0.90[ASN][1000 genomes]
rs1978593	0.88[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28454662	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28469789	0.91[AFR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28635243	0.88[EUR][1000 genomes]
rs35116687	0.88[AFR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35610141	0.90[AFR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4418303	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4947747	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60716577	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67604530	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6958886	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7777290	0.91[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7790364	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7790712	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7806644	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9690428	0.90[AFR][1000 genomes];0.91[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	nsv888026	chr7:52588348-53013671	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1019722	chr7:52767403-52800721	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv538842	chr7:52767403-52800721	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:52783800-52787400	Weak transcription	Pancreas	Pancrea
2	chr7:52785400-52785600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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