Variant report

Variant	rs61113828
Chromosome Location	chr8:119316288-119316289
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1843536	0.83[ASN][1000 genomes]
rs28365508	0.95[ASN][1000 genomes]
rs28365509	0.95[ASN][1000 genomes]
rs28365511	0.95[ASN][1000 genomes]
rs28365513	0.95[ASN][1000 genomes]
rs28365514	0.95[ASN][1000 genomes]
rs28365515	0.90[ASN][1000 genomes]
rs28365519	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3894436	0.93[ASN][1000 genomes]
rs55779460	1.00[ASN][1000 genomes]
rs55969036	0.83[ASN][1000 genomes]
rs56067593	1.00[ASN][1000 genomes]
rs56786266	0.95[ASN][1000 genomes]
rs57136694	0.83[ASN][1000 genomes]
rs57452718	0.95[ASN][1000 genomes]
rs57969351	0.93[ASN][1000 genomes]
rs58198250	0.83[ASN][1000 genomes]
rs58351047	1.00[ASN][1000 genomes]
rs58457489	0.83[ASN][1000 genomes]
rs58533762	1.00[ASN][1000 genomes]
rs58915741	0.83[ASN][1000 genomes]
rs60224208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60268410	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60421047	0.86[ASN][1000 genomes]
rs60914960	1.00[ASN][1000 genomes]
rs67252252	1.00[ASN][1000 genomes]
rs7005199	1.00[ASN][1000 genomes]
rs7007277	1.00[ASN][1000 genomes]
rs72675876	1.00[ASN][1000 genomes]
rs72675877	1.00[ASN][1000 genomes]
rs73320255	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73320264	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73320273	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73321948	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73321952	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73321972	1.00[ASN][1000 genomes]
rs7464659	1.00[ASN][1000 genomes]
rs7817037	1.00[ASN][1000 genomes]
rs7846246	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612047	chr8:118939094-119468609	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1015380	chr8:118948652-119418389	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv539736	chr8:118948652-119418389	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1032681	chr8:119153316-119609948	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv539737	chr8:119153316-119609948	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv1016379	chr8:119164234-119448910	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
7	nsv831442	chr8:119181675-119390122	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119304200-119322200	Weak transcription	GM12878-XiMat	blood
2	chr8:119315400-119316400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
3	chr8:119315400-119316400	Enhancers	Right Atrium	heart
4	chr8:119315800-119316400	Enhancers	Fetal Lung	lung
5	chr8:119316000-119316400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:119316000-119316400	Enhancers	Aorta	Aorta
7	chr8:119316000-119316400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
8	chr8:119316000-119318200	Weak transcription	Fetal Brain Male	brain
9	chr8:119316200-119316400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:119316200-119316400	Enhancers	Brain Angular Gyrus	brain
11	chr8:119316200-119316400	Enhancers	Brain Substantia Nigra	brain
12	chr8:119316200-119316400	Enhancers	Fetal Stomach	stomach
13	chr8:119316200-119316400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:119316200-119316600	Enhancers	Brain Cingulate Gyrus	brain
15	chr8:119316200-119317000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:119316200-119317400	Weak transcription	Brain Hippocampus Middle	brain

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