Variant report

Variant	rs2836462
Chromosome Location	chr21:39895800-39895801
allele	A/G
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:12)

rs_ID	r²[population]
rs11908941	0.87[ASW][hapmap]
rs11909285	1.00[EUR][1000 genomes]
rs11909765	0.87[ASW][hapmap]
rs17193990	1.00[EUR][1000 genomes]
rs2836457	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2836460	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2836461	1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836465	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2836467	0.87[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2836468	0.83[ASN][1000 genomes]
rs2836470	1.00[CHD][hapmap];0.83[ASN][1000 genomes]
rs3787911	0.80[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39892000-39896000	Enhancers	HepG2	liver
2	chr21:39892600-39896000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr21:39893600-39896400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr21:39895400-39895800	Enhancers	Aorta	Aorta
5	chr21:39895400-39896200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr21:39895800-39896000	Enhancers	Small Intestine	intestine
7	chr21:39895800-39896000	Bivalent Enhancer	Osteobl	bone
8	chr21:39895800-39897200	Weak transcription	Aorta	Aorta

Quick Search:

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

what's new

Quick links