Variant report

Variant	rs61428202
Chromosome Location	chr8:113734415-113734416
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11985496	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11993017	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11995039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16883975	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16884126	1.00[AMR][1000 genomes]
rs16884129	1.00[AMR][1000 genomes]
rs57873127	0.91[AFR][1000 genomes]
rs58296437	0.91[AFR][1000 genomes]
rs59464748	0.91[AFR][1000 genomes]
rs60598285	0.91[AFR][1000 genomes]
rs73700802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73702203	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73702223	0.91[AFR][1000 genomes]
rs73702225	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv534270	chr8:113585830-113979075	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113733800-113735000	Enhancers	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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