Variant report

Variant	rs11779602
Chromosome Location	chr8:66462482-66462483
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11776874	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11776926	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11779601	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11781358	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11782837	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11783633	0.84[EUR][1000 genomes]
rs11783755	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13261559	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13262793	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17396080	0.82[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761434	chr8:65578467-66567678	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66461600-66462600	Enhancers	Fetal Brain Male	brain
2	chr8:66462000-66462600	Enhancers	Fetal Brain Female	brain
3	chr8:66462200-66462600	Enhancers	Brain Germinal Matrix	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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