Variant report

Variant	rs7559441
Chromosome Location	chr2:33678331-33678332
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10173760	0.88[CEU][hapmap]
rs10779917	0.88[CEU][hapmap]
rs11124317	0.88[CEU][hapmap];0.81[MEX][hapmap];0.86[TSI][hapmap]
rs12612879	0.82[CEU][hapmap]
rs1455943	0.83[CEU][hapmap]
rs1531125	0.88[CEU][hapmap]
rs1979241	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs1979242	0.88[CEU][hapmap];0.97[GIH][hapmap];0.81[MEX][hapmap];0.96[TSI][hapmap];0.89[EUR][1000 genomes]
rs2008255	1.00[ASW][hapmap];0.88[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2124437	0.81[CHB][hapmap]
rs6728868	0.81[CHB][hapmap];0.94[GIH][hapmap];0.85[TSI][hapmap]
rs6756871	0.88[CEU][hapmap]
rs6756915	0.88[CEU][hapmap]
rs6756985	0.88[CEU][hapmap]

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	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33668800-33685200	Weak transcription	HUVEC	blood vessel
2	chr2:33677600-33679400	ZNF genes & repeats	Fetal Muscle Leg	muscle
3	chr2:33678200-33679400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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