Variant report

Variant	rs11714137
Chromosome Location	chr3:155750273-155750274
allele	C/G
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]
rs11719280	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs1850283	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs34533513	0.98[EUR][1000 genomes]
rs4680230	0.99[EUR][1000 genomes]
rs6441032	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6776718	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6806030	0.83[EUR][1000 genomes]
rs6806441	0.93[EUR][1000 genomes]
rs71310459	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7643130	0.95[EUR][1000 genomes]
rs883670	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155749000-155751000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:155749000-155751000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:155749400-155751200	Weak transcription	H9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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