Variant report

Variant	rs657134
Chromosome Location	chr1:84471653-84471654
allele	C/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]
rs2477201	0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs558567	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs575633	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs587007	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs598531	0.85[ASN][1000 genomes]
rs639666	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs685472	0.81[ASN][1000 genomes]
rs686839	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84468400-84473800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:84468600-84473800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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