Variant report

Variant	rs12670625
Chromosome Location	chr7:103627907-103627908
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12667402	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12667559	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12669862	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12674214	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2188245	1.00[CEU][hapmap]
rs4729962	1.00[CEU][hapmap]
rs73185420	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103626600-103629000	Active TSS	HepG2	liver
2	chr7:103627600-103628000	Transcr. at gene 5' and 3'	K562	blood
3	chr7:103627800-103628000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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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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