Variant report

Variant	rs9370833
Chromosome Location	chr6:15853923-15853924
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]
rs10484349	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12192897	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12209943	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7349936	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs742383	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7751000	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7751282	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9367884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9370834	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9476963	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15843000-15855400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:15850600-15855400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr6:15850800-15855400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:15850800-15855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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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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