Variant report

Variant	rs529243
Chromosome Location	chr1:166754090-166754091
allele	C/T
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:11)

rs_ID	r²[population]
rs499528	1.00[AMR][1000 genomes]
rs525075	1.00[AMR][1000 genomes]
rs542163	1.00[AMR][1000 genomes]
rs555321	1.00[AMR][1000 genomes]
rs565810	1.00[AMR][1000 genomes]
rs566924	1.00[AMR][1000 genomes]
rs572523	1.00[AMR][1000 genomes]
rs577003	1.00[AMR][1000 genomes]
rs577172	1.00[AMR][1000 genomes]
rs577252	1.00[AMR][1000 genomes]
rs577965	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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166753600-166754400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:166753600-166754600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:166753600-166755400	Enhancers	H9 Cell Line	embryonic stem cell
4	chr1:166753800-166754400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:166753800-166754400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:166753800-166754400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:166754000-166754400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr1:166754000-166754400	Flanking Active TSS	HUES6 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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