Variant report

Variant	rs7006199
Chromosome Location	chr8:85093558-85093559
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10088407	1.00[AMR][1000 genomes]
rs10093509	1.00[AMR][1000 genomes]
rs10096837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57108863	1.00[AMR][1000 genomes]
rs73302441	1.00[AMR][1000 genomes]
rs73689607	1.00[AMR][1000 genomes]
rs7825336	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	esv2753846	chr8:84637092-85239703	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv611646	chr8:85048690-85112377	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr8:85088800-85094000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr8:85092800-85093600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr8:85092800-85094400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:85093000-85093800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:85093000-85093800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:85093400-85093800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:85093400-85094000	Bivalent Enhancer	HUES64 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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