Variant report

Variant	rs34087014
Chromosome Location	chr13:93105862-93105863
allele	C/T
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]
rs12865759	1.00[EUR][1000 genomes]
rs34004765	1.00[EUR][1000 genomes]
rs34022722	1.00[EUR][1000 genomes]
rs34322289	1.00[EUR][1000 genomes]
rs35352976	1.00[EUR][1000 genomes]
rs35629298	1.00[EUR][1000 genomes]
rs35970869	1.00[EUR][1000 genomes]
rs71427573	1.00[EUR][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	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93105200-93106000	Enhancers	Fetal Brain Female	brain
2	chr13:93105200-93106200	Active TSS	Ovary	ovary
3	chr13:93105600-93106000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:93105600-93106000	Active TSS	Muscle Satellite Cultured Cells	--
5	chr13:93105800-93114800	Weak transcription	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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