Variant report

Variant	rs60182967
Chromosome Location	chr6:133699266-133699267
allele	C/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]
rs3777840	1.00[AMR][1000 genomes]
rs3777846	1.00[AMR][1000 genomes]
rs3822933	1.00[AMR][1000 genomes]
rs73559619	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73559628	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73559630	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73559632	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73559633	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73559634	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73559647	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9493608	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133684600-133717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:133691400-133700200	Weak transcription	Psoas Muscle	Psoas
3	chr6:133691400-133700800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:133691600-133701200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr6:133698000-133699400	Enhancers	Hela-S3	cervix
6	chr6:133698600-133700200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:133698800-133700800	Weak transcription	HSMMtube	muscle

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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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