Variant report

Variant	rs10778265
Chromosome Location	chr12:103977261-103977262
allele	G/T
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]
rs10454504	0.98[EUR][1000 genomes]
rs10745975	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10778266	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10861042	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10861043	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11111671	0.96[EUR][1000 genomes]
rs11836449	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12319902	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs903186	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103976800-103977400	Enhancers	HMEC	breast

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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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