Variant report

Variant	rs73691532
Chromosome Location	chr8:67300192-67300193
allele	A/T
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]
rs16932729	1.00[AMR][1000 genomes]
rs16932854	0.81[AFR][1000 genomes]
rs1961321	0.81[AFR][1000 genomes]
rs57240176	0.81[AFR][1000 genomes]
rs57303455	1.00[AMR][1000 genomes]
rs59180218	1.00[AMR][1000 genomes]
rs59891340	1.00[AMR][1000 genomes]
rs61201861	1.00[AMR][1000 genomes]
rs73691533	0.81[AFR][1000 genomes]
rs73691535	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691541	1.00[AMR][1000 genomes]
rs73691542	0.82[AFR][1000 genomes];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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67291000-67304000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:67293000-67300200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr8:67295800-67300200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:67295800-67301000	Weak transcription	Right Atrium	heart
5	chr8:67298200-67300200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:67299400-67301200	Enhancers	Fetal Heart	heart

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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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