Variant report

Variant	rs6990901
Chromosome Location	chr8:34716641-34716642
allele	A/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:6)

rs_ID	r²[population]
rs11987573	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11994213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73580160	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73580163	0.82[AFR][1000 genomes]
rs73580164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73580167	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3693375	chr8:34631970-34780509	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv972208	chr8:34644254-34790092	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv890716	chr8:34707436-34822797	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr8:34708800-34717400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:34715000-34717000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr8:34715000-34718000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:34715000-34718000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:34716600-34717000	Weak transcription	iPS-20b 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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