Variant report

Variant	rs7560091
Chromosome Location	chr2:172361475-172361476
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]
rs12053287	1.00[CEU][hapmap]
rs16823212	1.00[EUR][1000 genomes]
rs16859549	1.00[CEU][hapmap]
rs17287442	1.00[CHD][hapmap]
rs2017090	1.00[JPT][hapmap]
rs2674496	1.00[EUR][1000 genomes]
rs3731979	1.00[EUR][1000 genomes]
rs3795997	1.00[EUR][1000 genomes]
rs56392714	1.00[EUR][1000 genomes]
rs57136707	1.00[EUR][1000 genomes]
rs57580465	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59827170	1.00[EUR][1000 genomes]
rs60018506	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62183543	1.00[ASN][1000 genomes]
rs6729749	1.00[EUR][1000 genomes]
rs6730160	1.00[EUR][1000 genomes]
rs73976160	1.00[EUR][1000 genomes]
rs73976165	1.00[EUR][1000 genomes]
rs73976170	1.00[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	esv3382346	chr2:172062677-172363892	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	esv1832950	chr2:172283513-172488111	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr2:172340000-172368400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:172360600-172365600	Weak transcription	Small Intestine	intestine
3	chr2:172361200-172363600	Enhancers	Foreskin Melanocyte Primary Cells skin03	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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