Variant report

Variant	rs16926974
Chromosome Location	chr8:62079122-62079123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16926861	1.00[EUR][1000 genomes]
rs16926875	1.00[EUR][1000 genomes]
rs16926901	1.00[EUR][1000 genomes]
rs16927039	1.00[EUR][1000 genomes]
rs16927148	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16927151	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16927168	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv465698	chr8:62036793-62179465	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv611426	chr8:62036793-62179465	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1026243	chr8:62039073-62101123	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv890949	chr8:62073346-62141341	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62063000-62084600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:62068200-62084200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:62077000-62084000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:62077200-62079800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr8:62078200-62080400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:62078400-62080800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:62078400-62080800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:62078800-62079800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:62079000-62080400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr8:62079000-62082200	Weak transcription	iPS-18 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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