Variant report

Variant	rs11801198
Chromosome Location	chr1:47297679-47297680
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1105456	0.91[YRI][hapmap];0.86[AFR][1000 genomes]
rs11803239	0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11811700	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12026027	1.00[EUR][1000 genomes]
rs12036374	1.00[EUR][1000 genomes]
rs12062956	1.00[JPT][hapmap]
rs12563793	0.83[EUR][1000 genomes]
rs4294366	1.00[JPT][hapmap]
rs45464595	1.00[EUR][1000 genomes]
rs45468297	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs45470393	0.85[AFR][1000 genomes]
rs45626036	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4646476	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs4646477	1.00[EUR][1000 genomes]
rs4646488	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs4646494	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs4646496	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs57200251	1.00[EUR][1000 genomes]
rs57557506	1.00[EUR][1000 genomes]
rs58223210	1.00[EUR][1000 genomes]
rs58445319	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58826184	1.00[EUR][1000 genomes]
rs58929824	1.00[EUR][1000 genomes]
rs59838435	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1013048	chr1:47132831-47377364	Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv534955	chr1:47132831-47377364	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1011086	chr1:47259078-47305191	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv870538	chr1:47259138-47309265	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1004143	chr1:47270942-47321982	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1004246	chr1:47274901-47321982	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv947111	chr1:47277189-47308420	ZNF genes & repeats Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr1:47289000-47301200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr1:47289200-47308200	Weak transcription	Adipose Nuclei	Adipose
3	chr1:47296800-47300400	Weak transcription	Lung	lung
4	chr1:47297000-47300000	Weak transcription	Esophagus	oesophagus

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