Variant report

Variant	rs62472599
Chromosome Location	chr7:83988132-83988133
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10236082	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10255354	0.81[ASN][1000 genomes]
rs10954752	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10954753	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11972641	0.82[ASN][1000 genomes]
rs12707647	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13238916	0.82[ASN][1000 genomes]
rs13437800	0.82[AMR][1000 genomes]
rs13437801	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1974512	0.82[ASN][1000 genomes]
rs1987325	0.82[ASN][1000 genomes]
rs2158169	0.82[ASN][1000 genomes]
rs2189119	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2372453	0.82[ASN][1000 genomes]
rs2372454	0.82[ASN][1000 genomes]
rs2522371	0.82[ASN][1000 genomes]
rs2681435	0.82[ASN][1000 genomes]
rs2888321	0.82[ASN][1000 genomes]
rs4728554	0.82[ASN][1000 genomes]
rs4732548	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4732549	0.82[ASN][1000 genomes]
rs519663	0.82[ASN][1000 genomes]
rs521595	0.82[ASN][1000 genomes]
rs524163	0.82[ASN][1000 genomes]
rs524301	0.82[ASN][1000 genomes]
rs539643	0.81[ASN][1000 genomes]
rs540454	0.82[ASN][1000 genomes]
rs549975	0.82[ASN][1000 genomes]
rs560627	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs568973	0.82[ASN][1000 genomes]
rs607120	0.82[ASN][1000 genomes]
rs608459	0.82[ASN][1000 genomes]
rs609308	0.82[ASN][1000 genomes]
rs611442	0.82[ASN][1000 genomes]
rs611503	0.82[ASN][1000 genomes]
rs612337	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs612856	0.82[ASN][1000 genomes]
rs613335	0.82[ASN][1000 genomes]
rs620892	0.82[ASN][1000 genomes]
rs621903	0.82[ASN][1000 genomes]
rs623289	0.82[ASN][1000 genomes]
rs62472600	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62472601	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62472602	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62472603	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs633234	0.82[ASN][1000 genomes]
rs642572	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs648653	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs650395	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7789787	0.82[ASN][1000 genomes]
rs7808081	0.82[ASN][1000 genomes]
rs961201	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv2754468	chr7:83851249-84166749	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv1793815	chr7:83909503-83997755	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv888631	chr7:83911271-84010005	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv888632	chr7:83958436-83993099	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv1023848	chr7:83985028-84101774	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2761342	chr7:83985028-84101798	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr7:83985000-83994200	Weak transcription	NHDF-Ad	bronchial
2	chr7:83985400-83992800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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