Variant report

Variant	rs9396626
Chromosome Location	chr6:15990686-15990687
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]
rs4716020	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67091502	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6940301	0.90[ASN][1000 genomes]
rs72653739	0.87[ASN][1000 genomes]
rs9349991	0.87[ASN][1000 genomes]
rs9367887	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9370851	0.87[ASN][1000 genomes]
rs9370852	0.86[ASN][1000 genomes]
rs9370853	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9383097	0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15988000-15995000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:15988400-15991200	Weak transcription	K562	blood
3	chr6:15990600-15991000	Enhancers	GM12878-XiMat	blood

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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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