Variant report

Variant	rs73317522
Chromosome Location	chr12:64947649-64947650
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs56721582	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60878922	1.00[AMR][1000 genomes]
rs73317530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73317532	1.00[AFR][1000 genomes];1.00[AMR][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	nsv832443	chr12:64878856-65057265	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription 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	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64944800-64954000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:64946400-64952600	Weak transcription	Fetal Muscle Leg	muscle
3	chr12:64947200-64948200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr12:64947400-64948400	Weak transcription	Adipose Nuclei	Adipose
5	chr12:64947600-64948800	Enhancers	HepG2	liver

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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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