Variant report

Variant	rs55993114
Chromosome Location	chr14:42430159-42430160
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11539099	1.00[AMR][1000 genomes]
rs56176025	1.00[AMR][1000 genomes]
rs57469155	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59280798	1.00[AMR][1000 genomes]
rs61191609	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61438069	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74045462	1.00[AMR][1000 genomes]
rs74045713	0.94[AFR][1000 genomes];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	nsv901740	chr14:42386859-42477256	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 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	chr14:42430000-42430200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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