Variant report

Variant	rs28627679
Chromosome Location	chr1:220666500-220666501
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12562686	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13376101	0.85[AFR][1000 genomes]
rs17007796	0.85[EUR][1000 genomes]
rs57827085	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58948810	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60807411	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7516373	0.85[EUR][1000 genomes]
rs7530302	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220665600-220666800	Enhancers	Pancreas	Pancrea
2	chr1:220666200-220667200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:220666400-220667000	Enhancers	Adipose Nuclei	Adipose

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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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