Variant report

Variant	rs4655295
Chromosome Location	chr1:213700727-213700728
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:32)

rs_ID	r²[population]
rs1078308	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10864049	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10864050	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120151	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11120152	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120153	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120154	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12027967	0.88[AFR][1000 genomes]
rs1391870	0.87[ASN][1000 genomes]
rs1532535	0.87[ASN][1000 genomes]
rs2165131	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2501457	0.87[ASN][1000 genomes]
rs320388	0.86[ASN][1000 genomes]
rs320390	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs320393	0.87[ASN][1000 genomes]
rs320422	1.00[ASN][1000 genomes]
rs320424	1.00[ASN][1000 genomes]
rs320426	0.86[ASN][1000 genomes]
rs383945	1.00[ASN][1000 genomes]
rs393105	0.87[ASN][1000 genomes]
rs401923	0.87[ASN][1000 genomes]
rs410108	0.87[ASN][1000 genomes]
rs433540	0.83[EUR][1000 genomes]
rs4655294	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655446	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655447	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655448	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs893665	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs893666	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs920355	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs920356	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs920357	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832525	chr1:213580476-213782815	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr1:213698000-213703800	Weak transcription	Right Ventricle	heart
2	chr1:213700000-213703600	Weak transcription	Fetal Heart	heart
3	chr1:213700400-213703600	Weak transcription	Fetal Lung	lung

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