Variant report

Variant	rs167109
Chromosome Location	chr11:86088687-86088688
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11234628	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs148574	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17149021	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs292094	0.87[AFR][1000 genomes]
rs292096	0.86[AFR][1000 genomes]
rs292097	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs292098	0.94[EUR][1000 genomes]
rs292101	0.88[AFR][1000 genomes]
rs292102	0.88[AFR][1000 genomes]
rs292103	0.87[AFR][1000 genomes]
rs292105	0.87[AFR][1000 genomes]
rs292106	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs292107	0.95[EUR][1000 genomes]
rs292111	0.96[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86084400-86089200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:86086000-86102200	Weak transcription	Left Ventricle	heart
3	chr11:86086000-86106200	Weak transcription	Aorta	Aorta
4	chr11:86086200-86091200	Weak transcription	HUVEC	blood vessel

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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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