Variant report

Variant	rs7452880
Chromosome Location	chr6:71984238-71984239
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10945297	0.81[AMR][1000 genomes]
rs6908858	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6935716	0.90[AFR][1000 genomes]
rs8180646	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9342827	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9346452	0.81[AMR][1000 genomes]
rs9354985	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9360443	0.83[ASN][1000 genomes]
rs9360444	0.81[AMR][1000 genomes]
rs9364148	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9364149	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	chr6:71979400-71988200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:71980800-71987800	Weak transcription	H1 Derived Mesenchymal Stem 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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