Variant report

Variant	rs6431652
Chromosome Location	chr2:234918391-234918392
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1118259	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2052029	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2052030	1.00[CEU][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2190951	0.96[CEU][hapmap];0.82[CHD][hapmap];1.00[MEX][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4664000	0.92[CEU][hapmap];0.84[CHB][hapmap];0.82[JPT][hapmap];0.93[YRI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4664001	0.96[CEU][hapmap];0.82[CHD][hapmap];1.00[MEX][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs585284	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs601129	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs604082	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6431650	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6431651	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6721761	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs6727222	1.00[CHB][hapmap];0.80[JPT][hapmap];0.93[YRI][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6734618	0.92[CEU][hapmap];0.91[CHB][hapmap];0.96[CHD][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7560562	0.91[CHB][hapmap];0.90[CHD][hapmap];0.87[JPT][hapmap];0.82[MEX][hapmap];0.88[YRI][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7576321	0.86[AMR][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	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 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	chr2:234909600-234919000	Strong transcription	Liver	Liver
2	chr2:234914200-234919600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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