Variant report

Variant	rs11777607
Chromosome Location	chr8:52244927-52244928
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10091690	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1123900	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11774588	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11775272	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11777020	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11777663	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11780044	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11780126	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11780926	0.91[EUR][1000 genomes]
rs11782525	0.91[EUR][1000 genomes]
rs11786018	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11786053	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11787070	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11787165	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17176316	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2392834	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2392835	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7005870	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv948338	chr8:52060314-52368754	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv890895	chr8:52190571-52615191	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52240800-52245000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:52244200-52245000	Enhancers	Left Ventricle	heart

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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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