Variant report

Variant	rs10266093
Chromosome Location	chr7:138034900-138034901
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10236236	1.00[AMR][1000 genomes]
rs10240379	1.00[AMR][1000 genomes]
rs10242949	1.00[AMR][1000 genomes]
rs10258211	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10263190	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10264150	1.00[AMR][1000 genomes]
rs10264232	1.00[AMR][1000 genomes]
rs10271111	1.00[AMR][1000 genomes]
rs11971525	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11975661	1.00[AMR][1000 genomes]
rs12334219	1.00[AMR][1000 genomes]
rs28455808	1.00[AMR][1000 genomes]
rs28541317	1.00[AMR][1000 genomes]
rs28620635	1.00[AMR][1000 genomes]
rs28678352	1.00[AMR][1000 genomes]
rs28767250	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28810494	1.00[AMR][1000 genomes]
rs28874637	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	esv3348355	chr7:138022746-138072487	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	1 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	chr7:138033800-138035200	Enhancers	Fetal Brain Male	brain
2	chr7:138034400-138038800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr7:138034600-138036800	ZNF genes & repeats	K562	blood

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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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