Variant report

Variant	rs73573712
Chromosome Location	chr8:49073779-49073780
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17287584	1.00[AMR][1000 genomes]
rs45531731	1.00[AMR][1000 genomes]
rs73571643	1.00[AMR][1000 genomes]
rs73573731	0.91[AFR][1000 genomes]
rs73573734	0.91[AFR][1000 genomes]
rs73573737	0.80[AFR][1000 genomes]
rs73577390	1.00[AMR][1000 genomes]
rs73579436	1.00[AMR][1000 genomes]
rs73579442	1.00[AMR][1000 genomes]
rs8178070	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	nsv931032	chr8:48744329-49091359	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49073200-49074400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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