Variant report

Variant	rs4603367
Chromosome Location	chr12:45861909-45861910
allele	C/G
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:19)

rs_ID	r²[population]
rs10748424	0.84[CEU][hapmap]
rs10880795	0.83[EUR][1000 genomes]
rs11183055	0.92[EUR][1000 genomes]
rs11183063	0.84[EUR][1000 genomes]
rs12366559	0.92[EUR][1000 genomes]
rs12367751	0.92[EUR][1000 genomes]
rs17096106	0.89[JPT][hapmap]
rs2408252	0.80[EUR][1000 genomes]
rs2408261	0.89[JPT][hapmap]
rs2408273	0.83[EUR][1000 genomes]
rs2408319	0.83[EUR][1000 genomes]
rs4269980	0.89[JPT][hapmap]
rs4408369	0.80[EUR][1000 genomes]
rs4444141	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs4576884	0.83[EUR][1000 genomes]
rs6582555	0.83[EUR][1000 genomes]
rs7312557	0.85[EUR][1000 genomes]
rs7315711	0.92[EUR][1000 genomes]
rs7964616	0.83[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	nsv832395	chr12:45841765-46039297	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	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	chr12:45861800-45865800	Enhancers	Fetal Thymus	thymus

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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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