Variant report

Variant	rs2600655
Chromosome Location	chr5:4973759-4973760
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10038746	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10038747	0.88[EUR][1000 genomes]
rs1035914	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1452027	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs181822	0.81[ASN][1000 genomes]
rs189835	0.89[EUR][1000 genomes]
rs1901498	0.92[EUR][1000 genomes]
rs2399756	0.89[EUR][1000 genomes]
rs249457	0.81[ASN][1000 genomes]
rs2561719	0.92[EUR][1000 genomes]
rs2561720	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2561721	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2561722	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs30450	0.81[ASN][1000 genomes]
rs30462	0.81[ASN][1000 genomes]
rs30463	0.81[ASN][1000 genomes]
rs30472	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs30473	0.84[EUR][1000 genomes]
rs30474	0.90[EUR][1000 genomes]
rs30475	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs374207	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs39586	0.91[EUR][1000 genomes]
rs39850	0.81[ASN][1000 genomes]
rs39853	0.91[EUR][1000 genomes]
rs40468	0.84[EUR][1000 genomes]
rs42400	0.90[EUR][1000 genomes]
rs42401	0.91[EUR][1000 genomes]
rs42545	0.91[EUR][1000 genomes]
rs42546	0.88[EUR][1000 genomes]
rs719183	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9313095	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs935857	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs935858	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019579	chr5:4557477-4997411	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1021653	chr5:4932992-5201887	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1028717	chr5:4954566-4993583	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 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	chr5:4970400-4976800	Weak transcription	Fetal Lung	lung
2	chr5:4973600-4974200	Enhancers	Fetal Kidney	kidney

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