Variant report

Variant	rs9304345
Chromosome Location	chr18:44871276-44871277
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1019989	0.94[ASW][hapmap];0.81[GIH][hapmap];0.95[LWK][hapmap];0.95[MKK][hapmap];0.88[TSI][hapmap];0.93[YRI][hapmap]
rs12458974	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7235455	0.94[ASW][hapmap];0.81[GIH][hapmap];0.95[LWK][hapmap];0.95[MKK][hapmap];0.88[TSI][hapmap];0.96[YRI][hapmap]
rs7244673	0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs752649	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8088668	0.95[AFR][1000 genomes]
rs9958618	0.93[AFR][1000 genomes];0.81[EUR][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	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44868800-44872000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr18:44869200-44872400	Enhancers	NHDF-Ad	bronchial

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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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