Variant report

Variant	rs28706123
Chromosome Location	chr4:119779512-119779513
allele	A/G
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]
rs10014331	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10019751	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11730732	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11944285	0.96[ASN][1000 genomes]
rs2052769	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28469651	0.92[ASN][1000 genomes]
rs28783784	0.98[ASN][1000 genomes]
rs6848274	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs767193	0.92[ASN][1000 genomes]
rs9884928	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs992463	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119772400-119788200	Weak transcription	NHDF-Ad	bronchial
2	chr4:119776600-119781800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:119779200-119779600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr4:119779200-119780200	Enhancers	Ovary	ovary

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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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