Variant report

Variant	rs9463427
Chromosome Location	chr6:48513128-48513129
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10456586	0.80[ASN][1000 genomes]
rs10456587	0.80[ASN][1000 genomes]
rs10456588	0.80[ASN][1000 genomes]
rs10948414	0.80[ASN][1000 genomes]
rs12154015	0.80[ASN][1000 genomes]
rs12191301	0.80[ASN][1000 genomes]
rs1304387	0.80[ASN][1000 genomes]
rs1343442	0.88[ASN][1000 genomes]
rs1348410	0.80[ASN][1000 genomes]
rs1348412	0.80[ASN][1000 genomes]
rs1348413	0.80[ASN][1000 genomes]
rs1361864	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1373190	0.88[ASN][1000 genomes]
rs1443625	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1443632	0.85[ASN][1000 genomes]
rs1443633	0.88[ASN][1000 genomes]
rs1443634	0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1816833	0.88[ASN][1000 genomes]
rs1816834	0.88[ASN][1000 genomes]
rs1838196	0.85[ASN][1000 genomes]
rs1838306	0.80[ASN][1000 genomes]
rs1971606	0.88[ASN][1000 genomes]
rs1971607	0.87[ASN][1000 genomes]
rs2244408	0.88[ASN][1000 genomes]
rs2244425	0.88[ASN][1000 genomes]
rs2244429	0.88[ASN][1000 genomes]
rs2244782	0.88[ASN][1000 genomes]
rs2244785	0.88[ASN][1000 genomes]
rs2254843	0.88[ASN][1000 genomes]
rs2255241	0.88[ASN][1000 genomes]
rs2396866	0.80[ASN][1000 genomes]
rs2396867	0.80[ASN][1000 genomes]
rs2396870	0.88[ASN][1000 genomes]
rs2396872	0.82[ASN][1000 genomes]
rs2586807	0.88[ASN][1000 genomes]
rs2586828	0.87[ASN][1000 genomes]
rs2586829	0.87[ASN][1000 genomes]
rs2586830	0.87[ASN][1000 genomes]
rs2586833	0.85[ASN][1000 genomes]
rs2798754	0.87[ASN][1000 genomes]
rs2798764	0.88[ASN][1000 genomes]
rs2996259	0.87[ASN][1000 genomes]
rs2996260	0.87[ASN][1000 genomes]
rs2996261	0.87[ASN][1000 genomes]
rs2996262	0.88[ASN][1000 genomes]
rs2996264	0.87[ASN][1000 genomes]
rs2996268	0.88[ASN][1000 genomes]
rs3010505	0.88[ASN][1000 genomes]
rs3010508	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3010509	0.88[ASN][1000 genomes]
rs4451132	0.80[ASN][1000 genomes]
rs4510675	0.80[ASN][1000 genomes]
rs56365818	0.80[ASN][1000 genomes]
rs62410703	0.80[ASN][1000 genomes]
rs6933868	0.80[ASN][1000 genomes]
rs6934005	0.80[ASN][1000 genomes]
rs6934063	0.80[ASN][1000 genomes]
rs6934240	0.80[ASN][1000 genomes]
rs6934559	0.80[ASN][1000 genomes]
rs9357575	0.93[AFR][1000 genomes]
rs9463417	0.80[ASN][1000 genomes]
rs9463426	0.93[AFR][1000 genomes]
rs9473372	0.80[ASN][1000 genomes]
rs9473373	0.80[ASN][1000 genomes]
rs9473374	0.80[ASN][1000 genomes]
rs9473375	0.80[ASN][1000 genomes]
rs9473376	0.80[ASN][1000 genomes]
rs9473377	0.80[ASN][1000 genomes]
rs9473378	0.80[ASN][1000 genomes]
rs9473379	0.80[ASN][1000 genomes]
rs9473380	0.80[ASN][1000 genomes]
rs9473381	0.80[ASN][1000 genomes]
rs9473382	0.80[ASN][1000 genomes]
rs9473383	0.80[ASN][1000 genomes]
rs9473385	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv603035	chr6:47902243-48700995	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1033151	chr6:48067287-48797029	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538217	chr6:48067287-48797029	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv885877	chr6:48117685-48626930	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv917050	chr6:48168742-48578496	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv830657	chr6:48387714-48566656	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv462942	chr6:48480264-48598199	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv885878	chr6:48481466-48623408	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv830658	chr6:48497904-48632523	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:48512800-48513200	Enhancers	Pancreatic Islets	Pancreatic Islet

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