Variant report

Variant	rs3019220
Chromosome Location	chr11:93079177-93079178
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1004417	0.90[EUR][1000 genomes]
rs1456239	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1598546	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1598547	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1869913	0.88[EUR][1000 genomes]
rs1960665	0.88[EUR][1000 genomes]
rs1975819	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2124559	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2259469	0.84[EUR][1000 genomes]
rs2259630	0.84[EUR][1000 genomes]
rs2605575	0.87[EUR][1000 genomes]
rs2605576	0.90[EUR][1000 genomes]
rs2605577	0.82[EUR][1000 genomes]
rs2605578	0.85[EUR][1000 genomes]
rs2605579	0.83[EUR][1000 genomes]
rs2658771	0.87[EUR][1000 genomes]
rs2658774	0.90[EUR][1000 genomes]
rs2925353	0.90[EUR][1000 genomes]
rs2925359	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2925363	0.83[EUR][1000 genomes]
rs3019203	0.88[EUR][1000 genomes]
rs3019204	0.88[EUR][1000 genomes]
rs3019218	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3019219	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3019227	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3019229	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3019230	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3020055	0.80[EUR][1000 genomes]
rs3020070	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3020071	0.88[EUR][1000 genomes]
rs3020072	0.84[EUR][1000 genomes]
rs3020075	0.87[EUR][1000 genomes]
rs3020080	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[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	nsv1039134	chr11:92790000-93219942	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv438	chr11:93034411-93080513	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv898180	chr11:93045561-93082053	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv468793	chr11:93068163-93129893	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
6	esv3415313	chr11:93077221-93079448	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93064600-93081800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:93078600-93082000	Weak transcription	K562	blood

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