Variant report

Variant	rs2757757
Chromosome Location	chr6:70288755-70288756
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2572991	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2607730	0.94[ASN][1000 genomes]
rs2757758	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs310259	0.87[ASN][1000 genomes]
rs310260	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34857559	0.84[ASN][1000 genomes]
rs4707218	0.85[ASN][1000 genomes]
rs6904921	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs9351764	0.84[ASN][1000 genomes]
rs9364032	0.97[ASN][1000 genomes]
rs9364033	0.85[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70287800-70289000	Enhancers	HSMM	muscle
2	chr6:70288000-70288800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr6:70288000-70288800	Enhancers	HSMMtube	muscle
4	chr6:70288000-70289000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:70288400-70288800	Enhancers	NH-A	brain
6	chr6:70288600-70291800	Enhancers	Fetal Brain Male	brain

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