Variant report

Variant	rs4016106
Chromosome Location	chr7:84038269-84038270
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-4	chr7:84038231-84042095	ucscGeneNc_uc003uia_1

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1228866	0.85[ASN][1000 genomes]
rs1228868	0.85[ASN][1000 genomes]
rs1228951	0.87[ASN][1000 genomes]
rs1228956	0.87[ASN][1000 genomes]
rs1520102	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1634605	0.88[ASN][1000 genomes]
rs16887703	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1715518	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17158998	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17159006	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1922349	0.89[EUR][1000 genomes]
rs2214749	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2428807	0.87[ASN][1000 genomes]
rs2527522	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2527527	0.89[EUR][1000 genomes]
rs2527529	0.89[EUR][1000 genomes]
rs2527532	0.95[EUR][1000 genomes]
rs2527533	0.84[EUR][1000 genomes]
rs2527535	0.89[EUR][1000 genomes]
rs2527536	0.89[EUR][1000 genomes]
rs2527537	0.95[EUR][1000 genomes]
rs2527538	0.95[EUR][1000 genomes]
rs2706903	0.95[EUR][1000 genomes]
rs2706912	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2706913	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2706916	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2715032	0.95[EUR][1000 genomes]
rs2715044	0.95[EUR][1000 genomes]
rs2715045	0.95[EUR][1000 genomes]
rs2715046	0.89[EUR][1000 genomes]
rs2715047	0.85[EUR][1000 genomes]
rs2888322	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs520178	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs526991	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs529539	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs530698	0.85[ASN][1000 genomes]
rs531582	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs555632	0.82[ASN][1000 genomes]
rs559041	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56144625	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs561955	0.85[ASN][1000 genomes]
rs625480	0.85[ASN][1000 genomes]
rs73711542	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73711549	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7783073	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	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
4	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
5	nsv534431	chr7:84001059-84138511	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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