Variant report

Variant	rs73691533
Chromosome Location	chr8:67305708-67305709
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16932854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16932871	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17383243	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1961321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56747323	1.00[AMR][1000 genomes]
rs57240176	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60232161	1.00[AMR][1000 genomes]
rs734619	1.00[AMR][1000 genomes]
rs73691532	0.81[AFR][1000 genomes]
rs73691538	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691539	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9693831	1.00[AMR][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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3414665	chr8:66936816-67381935	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr8:67300200-67306200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:67301200-67307400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:67301800-67319800	Weak transcription	Aorta	Aorta
4	chr8:67304600-67311200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:67305600-67306200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links