Variant report

Variant	rs9464832
Chromosome Location	chr6:15811258-15811259
allele	A/T
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]
rs12192181	0.84[CEU][hapmap];0.81[MEX][hapmap]
rs12193135	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12207114	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12216459	0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4712257	0.84[CEU][hapmap];0.95[CHB][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap];0.81[EUR][1000 genomes]
rs4715998	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6935121	0.84[CEU][hapmap]
rs6940942	0.82[CHB][hapmap];0.89[CHD][hapmap];0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs742387	0.84[CEU][hapmap]
rs9476906	0.84[CEU][hapmap]
rs9476934	0.84[CEU][hapmap];0.95[CHB][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15800400-15816200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:15809800-15814800	Enhancers	Fetal Brain Male	brain
3	chr6:15810800-15812800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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