Variant report

Variant	rs73308925
Chromosome Location	chr14:78809693-78809694
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17107757	1.00[AMR][1000 genomes]
rs59836777	1.00[AMR][1000 genomes]
rs60295560	1.00[AMR][1000 genomes]
rs73314405	1.00[AMR][1000 genomes]
rs73316016	1.00[AMR][1000 genomes]
rs8016770	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78802200-78810000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:78808800-78810200	Weak transcription	Brain Germinal Matrix	brain
3	chr14:78809600-78810600	Enhancers	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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