Variant report

Variant	rs4896900
Chromosome Location	chr6:147337849-147337850
allele	C/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]
rs1112833	0.81[AMR][1000 genomes]
rs1881665	0.83[CEU][hapmap];0.84[CHB][hapmap]
rs4143745	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4896901	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6570785	0.94[ASN][1000 genomes]
rs6909765	0.92[ASN][1000 genomes]
rs7740816	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7741525	0.80[ASN][1000 genomes]
rs9386177	0.83[CEU][hapmap];0.84[CHB][hapmap]
rs9399593	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147336800-147338200	Enhancers	K562	blood
2	chr6:147337600-147338000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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