Variant report

Variant	rs72992687
Chromosome Location	chr11:74775598-74775599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11236293	1.00[ASN][1000 genomes]
rs12271960	1.00[ASN][1000 genomes]
rs12273852	1.00[ASN][1000 genomes]
rs12275050	1.00[ASN][1000 genomes]
rs12289885	1.00[ASN][1000 genomes]
rs12290239	1.00[ASN][1000 genomes]
rs12292428	1.00[ASN][1000 genomes]
rs12295546	1.00[ASN][1000 genomes]
rs1439677	1.00[ASN][1000 genomes]
rs35951757	1.00[AFR][1000 genomes]
rs7111955	1.00[ASN][1000 genomes]
rs72994528	1.00[ASN][1000 genomes]
rs73498736	1.00[ASN][1000 genomes]
rs73498737	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897918	chr11:74757641-74798928	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 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	chr11:74773800-74782200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:74775200-74777000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:74775400-74776600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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