Variant report

Variant	rs16858440
Chromosome Location	chr4:45379622-45379623
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1108423	0.94[ASN][1000 genomes]
rs12644052	0.89[ASN][1000 genomes]
rs28708848	0.82[AFR][1000 genomes]
rs28842612	0.82[AFR][1000 genomes]
rs28848502	0.92[AFR][1000 genomes]
rs3947624	1.00[ASN][1000 genomes]
rs41497647	1.00[ASN][1000 genomes]
rs4308401	0.89[ASN][1000 genomes]
rs4345223	0.89[ASN][1000 genomes]
rs4359946	0.89[ASN][1000 genomes]
rs4434289	0.89[ASN][1000 genomes]
rs4482803	0.89[ASN][1000 genomes]
rs4492036	0.89[ASN][1000 genomes]
rs4694803	0.89[ASN][1000 genomes]
rs4694804	0.89[ASN][1000 genomes]
rs4695101	0.89[ASN][1000 genomes]
rs4695109	0.89[ASN][1000 genomes]
rs6844212	0.89[ASN][1000 genomes]
rs7654664	0.89[ASN][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	nsv594104	chr4:45105210-45665828	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv594107	chr4:45338240-45436394	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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

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