Variant report

Variant	rs12631943
Chromosome Location	chr3:86353938-86353939
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12714654	0.80[EUR][1000 genomes]
rs12714655	0.80[EUR][1000 genomes]
rs1495886	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1512913	0.80[EUR][1000 genomes]
rs1512918	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2644216	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9310005	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9310006	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs932057	0.80[EUR][1000 genomes]
rs979472	0.93[ASN][1000 genomes]
rs9835087	0.93[ASN][1000 genomes]
rs9860570	0.80[EUR][1000 genomes]
rs9873692	0.89[AMR][1000 genomes];0.92[ASN][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	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877115	chr3:86278951-86554319	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr3:86353600-86354200	Enhancers	Fetal Brain Female	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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