Variant report

Variant	rs1634614
Chromosome Location	chr7:84040847-84040848
allele	C/T
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: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1228859	0.94[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1228860	0.94[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1228866	0.82[EUR][1000 genomes]
rs1228867	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1228868	0.80[EUR][1000 genomes]
rs1228875	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1228876	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1228878	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1228879	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1228880	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1228882	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1228883	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1228909	0.85[EUR][1000 genomes]
rs1228913	0.80[EUR][1000 genomes]
rs1228916	0.80[EUR][1000 genomes]
rs1228933	0.81[EUR][1000 genomes]
rs1228938	0.80[EUR][1000 genomes]
rs1228939	0.94[CEU][hapmap];0.82[YRI][hapmap];0.80[EUR][1000 genomes]
rs1228943	0.87[EUR][1000 genomes]
rs1228944	0.87[EUR][1000 genomes]
rs1228945	0.87[EUR][1000 genomes]
rs1228947	0.87[EUR][1000 genomes]
rs1228948	0.82[EUR][1000 genomes]
rs1228949	0.86[EUR][1000 genomes]
rs1228950	0.86[EUR][1000 genomes]
rs1228951	0.85[EUR][1000 genomes]
rs1228952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1228953	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1228954	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1228956	0.87[EUR][1000 genomes]
rs1228958	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1228959	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1228961	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1228963	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1228965	0.84[EUR][1000 genomes]
rs1228966	0.86[EUR][1000 genomes]
rs1234535	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1234538	0.87[EUR][1000 genomes]
rs1634605	0.87[EUR][1000 genomes]
rs1715510	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1733998	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1733999	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2079352	0.85[EUR][1000 genomes]
rs2428807	0.85[EUR][1000 genomes]
rs2428808	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2527528	0.87[EUR][1000 genomes]
rs2706902	0.85[EUR][1000 genomes]
rs2706907	0.85[EUR][1000 genomes]
rs505758	0.84[CEU][hapmap]
rs530698	0.82[EUR][1000 genomes]
rs561955	0.81[EUR][1000 genomes]
rs62474863	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs625480	0.82[EUR][1000 genomes]
rs916865	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][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:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84038800-84042800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:84039000-84043000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:84040000-84041200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:84040000-84041200	Enhancers	A549	lung
5	chr7:84040200-84041200	Enhancers	NHLF	lung
6	chr7:84040200-84041400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:84040600-84041000	Weak transcription	Osteobl	bone

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