Variant report

Variant	rs1543147
Chromosome Location	chr2:115942632-115942633
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]
rs10185352	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10187050	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10187556	0.88[ASN][1000 genomes]
rs12466330	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12474896	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12475000	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17044170	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17044209	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4849385	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4849386	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67070696	0.91[ASN][1000 genomes]
rs67201082	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs67300776	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs68044608	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7565369	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7566462	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7566796	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs973176	0.82[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	nsv1014713	chr2:115858427-116018055	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1001542	chr2:115920847-116082585	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr2:115932600-115946400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:115940600-115945400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:115942200-115949800	Weak transcription	Pancreas	Pancrea

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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