Variant report

Variant	rs6532828
Chromosome Location	chr4:100654792-100654793
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13123292	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17535623	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17535916	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17608848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2866168	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34849574	1.00[ASN][1000 genomes]
rs4699759	0.83[AMR][1000 genomes]
rs56184565	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58575263	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58961259	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6835927	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73832847	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs871321	0.94[CEU][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100654200-100655000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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