Variant report

Variant	rs74056659
Chromosome Location	chr14:65584034-65584035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17093570	1.00[AMR][1000 genomes]
rs59724943	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74056669	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74056671	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74056672	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74056676	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74056679	1.00[AMR][1000 genomes]

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	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 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	chr14:65583800-65585000	Enhancers	Psoas Muscle	Psoas
2	chr14:65583800-65585000	Enhancers	GM12878-XiMat	blood
3	chr14:65583800-65585400	Enhancers	Lung	lung

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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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