Variant report

Variant	rs12261707
Chromosome Location	chr10:4359834-4359835
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10904228	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10904229	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11252461	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11252462	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1926789	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58217195	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58966582	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7898047	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]

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	nsv894785	chr10:4306421-4372629	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs12261707	AKR1C4	cis	parietal	SCAN
rs12261707	FLJ45983	cis	cerebellum	SCAN
rs12261707	DTX3L	trans	lymphoblastoid	RTeQTL
rs12261707	DIP2C	cis	parietal	SCAN

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4357000-4360600	Enhancers	Fetal Lung	lung
2	chr10:4358800-4361600	Weak transcription	Ovary	ovary
3	chr10:4359000-4362800	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:4359000-4373400	Weak transcription	Right Atrium	heart
5	chr10:4359400-4364600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:4359800-4366200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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