Variant report

Variant	rs73915472
Chromosome Location	chr2:11806145-11806146
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:15)

rs_ID	r²[population]
rs35653499	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55911243	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57245099	1.00[AMR][1000 genomes]
rs58056834	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58288290	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61444193	1.00[AMR][1000 genomes]
rs73915461	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915462	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915465	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915469	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915470	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915474	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915475	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915478	1.00[AMR][1000 genomes]
rs73915479	0.85[AFR][1000 genomes];1.00[AMR][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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11780600-11807200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:11798200-11809800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:11800400-11809200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:11803200-11807400	Enhancers	Hela-S3	cervix
5	chr2:11805800-11806200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:11805800-11806400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:11806000-11806800	Bivalent Enhancer	HepG2	liver

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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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