Variant report

Variant	rs7656483
Chromosome Location	chr4:60554015-60554016
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11724853	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11733083	0.98[ASN][1000 genomes]
rs11736631	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1507137	0.86[ASN][1000 genomes]
rs1848192	0.97[ASN][1000 genomes]
rs1994114	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2035428	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2035583	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2128438	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4860757	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7677707	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760852	chr4:60424576-60863454	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv594254	chr4:60529232-60609054	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv980424	chr4:60543627-60561102	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:60552000-60554600	Weak transcription	Liver	Liver

Quick Search:

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

what's new

Quick links