Variant report

Variant	rs4817650
Chromosome Location	chr21:16480898-16480899
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]
rs1003427	0.82[EUR][1000 genomes]
rs1022450	0.82[EUR][1000 genomes]
rs2026849	0.82[EUR][1000 genomes]
rs2150369	0.80[EUR][1000 genomes]
rs2403877	0.83[EUR][1000 genomes]
rs2823061	0.87[EUR][1000 genomes]
rs2823062	0.84[EUR][1000 genomes]
rs2823065	0.82[EUR][1000 genomes]
rs2823066	0.81[EUR][1000 genomes]
rs4816486	0.84[EUR][1000 genomes]
rs719112	0.81[EUR][1000 genomes]
rs7282412	0.82[EUR][1000 genomes]
rs9978683	0.84[EUR][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	nsv834048	chr21:16324481-16489570	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv521517	chr21:16474158-16482643	Enhancers Weak transcription	Chromatin interactive region	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	chr21:16479800-16485200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:16480800-16481200	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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