Variant report

Variant	rs479363
Chromosome Location	chr1:47924113-47924114
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1680019	0.85[AFR][1000 genomes]
rs1765156	1.00[AFR][1000 genomes]
rs2622916	1.00[AMR][1000 genomes]
rs2820966	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs472993	0.95[AFR][1000 genomes]
rs4926868	0.95[AFR][1000 genomes]
rs495482	1.00[AFR][1000 genomes]
rs506329	0.95[AFR][1000 genomes]
rs522768	0.95[AFR][1000 genomes]
rs527133	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs527430	0.95[AFR][1000 genomes]
rs557101	1.00[AFR][1000 genomes]
rs567097	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6665542	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6676787	1.00[AMR][1000 genomes]
rs9436456	0.95[AFR][1000 genomes]
rs9436902	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1001779	chr1:47884229-48111485	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv871299	chr1:47889417-48057890	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv2755190	chr1:47907580-48048680	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47918000-47924800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:47921000-47925200	Weak transcription	Right Atrium	heart
3	chr1:47922800-47926400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:47923000-47924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:47923600-47925200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:47923600-47926400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr1:47923800-47925800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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