Variant report

Variant	rs604248
Chromosome Location	chr12:118186623-118186624
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs471231	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs477022	0.80[EUR][1000 genomes]
rs481593	0.81[EUR][1000 genomes]
rs510907	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs515398	0.83[EUR][1000 genomes]
rs570592	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs584654	0.81[EUR][1000 genomes]
rs614651	0.81[EUR][1000 genomes]
rs61937721	0.86[EUR][1000 genomes]
rs61937724	0.87[EUR][1000 genomes]
rs630460	0.81[EUR][1000 genomes]
rs630808	0.83[EUR][1000 genomes]
rs6490152	0.92[EUR][1000 genomes]
rs665540	0.80[EUR][1000 genomes]
rs675383	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv53849	chr12:118179174-118186925	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118186600-118187600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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