Variant report

Variant	rs7690472
Chromosome Location	chr4:62552151-62552152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10007614	0.81[AMR][1000 genomes]
rs10020698	0.92[ASN][1000 genomes]
rs11131340	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11131341	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11931258	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11936993	0.90[ASN][1000 genomes]
rs12233820	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12233859	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12507326	0.86[AMR][1000 genomes]
rs12642037	0.91[ASN][1000 genomes]
rs13115278	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs13142656	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1391320	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1497897	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1497899	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1497900	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1542834	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1587294	0.91[ASN][1000 genomes]
rs2036199	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2343526	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4552500	1.00[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4860422	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4860423	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4860424	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs57415754	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6820960	0.81[AMR][1000 genomes]
rs7687302	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7690118	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs996208	0.82[AMR][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	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1004815	chr4:62398737-62553769	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv537110	chr4:62398737-62553769	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr4:62538000-62553000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr4:62547800-62552200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:62549200-62560400	Weak transcription	Fetal Stomach	stomach

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