Variant report

Variant	rs73081521
Chromosome Location	chr5:41502463-41502464
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs57298536	0.81[AFR][1000 genomes]
rs57590605	0.81[AFR][1000 genomes]
rs59447468	0.81[AFR][1000 genomes]
rs59814375	0.81[AFR][1000 genomes]
rs60225001	0.96[AFR][1000 genomes]
rs60682637	0.81[AFR][1000 genomes]
rs60707515	0.81[AFR][1000 genomes]
rs6877857	0.81[AFR][1000 genomes]
rs73079787	0.83[AFR][1000 genomes]
rs73079796	0.96[AFR][1000 genomes]
rs73079798	0.96[AFR][1000 genomes]
rs73079799	0.96[AFR][1000 genomes]
rs73081505	0.96[AFR][1000 genomes]
rs73081511	0.96[AFR][1000 genomes]
rs73081512	1.00[AFR][1000 genomes]
rs73081518	1.00[AFR][1000 genomes]
rs73081519	1.00[AFR][1000 genomes]
rs73081522	1.00[AFR][1000 genomes]
rs73081525	1.00[AFR][1000 genomes]
rs73081527	1.00[AFR][1000 genomes]
rs73081530	1.00[AFR][1000 genomes]
rs73081536	1.00[AFR][1000 genomes]
rs73081539	0.85[AFR][1000 genomes]
rs73081544	0.81[AFR][1000 genomes]
rs73081549	0.81[AFR][1000 genomes]
rs73081560	0.81[AFR][1000 genomes]
rs73081564	0.81[AFR][1000 genomes]
rs73081567	0.81[AFR][1000 genomes]
rs73081569	0.81[AFR][1000 genomes]
rs73081571	0.81[AFR][1000 genomes]
rs73081574	0.81[AFR][1000 genomes]
rs73081580	0.81[AFR][1000 genomes]
rs73081589	0.81[AFR][1000 genomes]
rs73081590	0.81[AFR][1000 genomes]
rs73081593	0.81[AFR][1000 genomes]
rs73081595	0.81[AFR][1000 genomes]
rs73081599	0.81[AFR][1000 genomes]
rs7705479	0.81[AFR][1000 genomes]
rs7709077	1.00[AFR][1000 genomes]
rs7709197	1.00[AFR][1000 genomes]
rs7710332	1.00[AFR][1000 genomes]
rs7710721	1.00[AFR][1000 genomes]
rs7711043	1.00[AFR][1000 genomes]
rs7711241	1.00[AFR][1000 genomes]
rs7730181	0.81[AFR][1000 genomes]
rs7730189	0.81[AFR][1000 genomes]

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41494400-41504600	Weak transcription	Ovary	ovary
2	chr5:41495800-41507000	Weak transcription	Left Ventricle	heart
3	chr5:41497800-41504000	Enhancers	Fetal Heart	heart
4	chr5:41501600-41503000	Enhancers	Pancreatic Islets	Pancreatic Islet

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

New variant types
New dimension of annotation
New regulatory manner
More detailed annotation on variant overlapped TFBS
More extended data
New search manner

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links