Variant report

Variant	rs13017140
Chromosome Location	chr2:124764675-124764676
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12996212	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs17010758	1.00[ASW][hapmap]
rs17010759	1.00[ASW][hapmap]
rs17010772	1.00[AFR][1000 genomes]
rs17010972	1.00[ASW][hapmap]
rs17269024	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs34711614	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs71428132	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs71428134	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs71428135	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs951031	1.00[AFR][1000 genomes]
rs960536	1.00[ASW][hapmap]
rs960537	1.00[ASW][hapmap]

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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:124764600-124764800	Enhancers	hESC Derived CD184+ Endoderm 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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