Variant report

Variant	rs1276880
Chromosome Location	chr6:82362574-82362575
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1145880	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1145887	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1145889	0.84[AMR][1000 genomes]
rs1276879	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1276881	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1276882	0.85[AMR][1000 genomes]
rs1276883	0.84[AMR][1000 genomes]
rs1322896	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs912029	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9344203	0.82[AMR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82358000-82368000	Weak transcription	Fetal Heart	heart
2	chr6:82360200-82365200	Weak transcription	NHDF-Ad	bronchial
3	chr6:82361800-82367200	Weak transcription	Left Ventricle	heart

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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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