Variant report

Variant	rs73578070
Chromosome Location	chr16:79947215-79947216
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs16951915	1.00[AMR][1000 genomes]
rs7188448	1.00[AMR][1000 genomes]
rs73576025	1.00[AMR][1000 genomes]
rs73578063	0.82[AFR][1000 genomes]
rs9936120	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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 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	chr16:79938400-79949200	Weak transcription	Ovary	ovary
2	chr16:79944000-79948600	Weak transcription	Small Intestine	intestine
3	chr16:79944800-79952800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr16:79945000-79948600	Weak transcription	Fetal Lung	lung
5	chr16:79945200-79949200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr16:79945200-79952800	Weak transcription	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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