Variant report

Variant	rs4978609
Chromosome Location	chr9:117530319-117530320
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10733612	0.83[ASN][1000 genomes]
rs10739427	0.82[ASN][1000 genomes]
rs10759734	0.82[ASN][1000 genomes]
rs10817673	0.81[ASN][1000 genomes]
rs10982399	0.81[ASN][1000 genomes]
rs12335468	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12348862	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7038398	0.85[ASN][1000 genomes]
rs7854152	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117525800-117533000	Weak transcription	Aorta	Aorta
2	chr9:117529400-117530800	Enhancers	Fetal Intestine Small	intestine
3	chr9:117529400-117532600	Enhancers	Fetal Intestine Large	intestine
4	chr9:117529800-117533400	Weak transcription	Esophagus	oesophagus

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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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