Variant report

Variant	rs1926090
Chromosome Location	chr6:133763112-133763113
allele	A/G
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]
rs1012605	0.82[EUR][1000 genomes]
rs1336534	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs1889946	0.81[EUR][1000 genomes]
rs1889947	0.81[EUR][1000 genomes]
rs1932748	0.92[EUR][1000 genomes]
rs6899927	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6907872	1.00[CEU][hapmap]
rs760861	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs9373053	0.82[CEU][hapmap]
rs9385647	0.81[CEU][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133749800-133777600	Weak transcription	Hela-S3	cervix
2	chr6:133752400-133763400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:133756800-133772600	Weak transcription	Right Atrium	heart
4	chr6:133758400-133769000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr6:133761000-133765400	Weak transcription	Psoas Muscle	Psoas

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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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