Variant report

Variant	rs428351
Chromosome Location	chr5:35385600-35385601
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs165946	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs244778	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs244780	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs244781	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs32769	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs32772	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs32773	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs400888	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs401419	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs423851	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35385400-35385600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:35385400-35385800	Enhancers	Monocytes-CD14+_RO01746	blood

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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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