Variant report

Variant	rs7582832
Chromosome Location	chr2:234822867-234822868
allele	A/C
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:12)

rs_ID	r²[population]
rs1003756	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs1003757	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs10203291	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10519356	1.00[CEU][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13396996	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2017655	0.85[EUR][1000 genomes]
rs2108806	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2108807	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs4497869	0.83[AMR][1000 genomes]
rs4663984	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs735552	1.00[CEU][hapmap]
rs737635	0.83[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	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 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	chr2:234821800-234823000	Enhancers	Fetal Intestine Large	intestine

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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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