Variant report

Variant	rs4284776
Chromosome Location	chr2:212972333-212972334
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs13395352	1.00[ASN][1000 genomes]
rs1357127	0.91[EUR][1000 genomes]
rs2888038	0.91[EUR][1000 genomes]
rs4471839	0.93[EUR][1000 genomes]
rs4672635	0.86[EUR][1000 genomes]
rs61276593	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6730882	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72937800	0.93[EUR][1000 genomes]
rs72939804	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72939812	1.00[ASN][1000 genomes]
rs7558179	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7582302	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7591736	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7600270	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875802	chr2:212867291-213004603	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv875804	chr2:212891401-212997024	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 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	chr2:212971800-212972400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr2:212971800-212973600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:212971800-212973600	Weak transcription	Aorta	Aorta
4	chr2:212972200-212972800	Weak transcription	Fetal Intestine Large	intestine
5	chr2:212972200-212973600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr2:212972200-212975400	Weak transcription	ES-UCSF4 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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