Variant report

Variant	rs7030516
Chromosome Location	chr9:15004578-15004579
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs10114147	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10756632	0.84[EUR][1000 genomes]
rs10756640	0.94[ASN][1000 genomes]
rs10810307	0.84[EUR][1000 genomes]
rs10810308	0.83[EUR][1000 genomes]
rs10961811	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10961817	0.83[EUR][1000 genomes]
rs10961819	0.88[CEU][hapmap];0.85[GIH][hapmap];0.93[TSI][hapmap];0.89[EUR][1000 genomes]
rs10961820	0.86[EUR][1000 genomes]
rs12340301	0.83[EUR][1000 genomes]
rs1412720	0.82[AMR][1000 genomes]
rs1412724	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1464607	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1855140	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1880012	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1880013	0.85[EUR][1000 genomes]
rs2140322	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2140326	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4008009	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4382569	0.83[AMR][1000 genomes]
rs4535838	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4548277	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4553007	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs6415721	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6474876	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6474878	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7018678	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7020107	0.83[EUR][1000 genomes]
rs7026072	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7027560	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7028104	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs7028702	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7029010	0.98[ASN][1000 genomes]
rs7030620	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7037967	1.00[CEU][hapmap];0.93[GIH][hapmap];0.88[LWK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7040712	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7044666	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7048248	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7048509	0.84[CEU][hapmap];0.86[EUR][1000 genomes]
rs7848522	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7855093	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7857763	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7865132	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9298710	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9969815	0.81[AMR][1000 genomes];0.86[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	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv892620	chr9:14922877-15086021	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv892621	chr9:14928013-15043692	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2761503	chr9:14960217-15049343	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv892622	chr9:14960217-15055607	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14994400-15020000	Weak transcription	Brain Angular Gyrus	brain
2	chr9:14994600-15011200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr9:14994800-15020000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr9:15003200-15020000	Weak transcription	Brain Anterior Caudate	brain

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