Variant report

Variant	rs28548646
Chromosome Location	chr4:56147522-56147523
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17085437	1.00[AMR][1000 genomes]
rs28698466	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	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56144600-56147600	Enhancers	H1 Cell Line	embryonic stem cell
2	chr4:56146400-56148000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:56147000-56147800	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr4:56147000-56148000	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr4:56147200-56147600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
6	chr4:56147200-56147800	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr4:56147200-56151400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:56147400-56148000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:56147400-56148800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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