Variant report

Variant	rs73833248
Chromosome Location	chr3:50759431-50759432
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs17051012	1.00[AMR][1000 genomes]
rs17051016	1.00[AMR][1000 genomes]
rs17051017	1.00[AMR][1000 genomes]
rs17051404	1.00[AMR][1000 genomes]
rs4560294	1.00[AMR][1000 genomes]
rs55723661	1.00[AMR][1000 genomes]
rs55731480	1.00[AMR][1000 genomes]
rs55852678	1.00[AMR][1000 genomes]
rs56112107	1.00[AMR][1000 genomes]
rs56198179	1.00[AMR][1000 genomes]
rs56341000	1.00[AMR][1000 genomes]
rs56413944	1.00[AMR][1000 genomes]
rs57077411	1.00[AMR][1000 genomes]
rs57155820	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57867785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57987466	1.00[AMR][1000 genomes]
rs58231937	1.00[AMR][1000 genomes]
rs58854038	1.00[AMR][1000 genomes]
rs58911362	1.00[AMR][1000 genomes]
rs59065723	1.00[AMR][1000 genomes]
rs59337835	1.00[AMR][1000 genomes]
rs59340349	1.00[AMR][1000 genomes]
rs59486246	1.00[AMR][1000 genomes]
rs59749820	1.00[AMR][1000 genomes]
rs59944295	1.00[AMR][1000 genomes]
rs60209025	1.00[AMR][1000 genomes]
rs60420261	1.00[AMR][1000 genomes]
rs61032466	1.00[AMR][1000 genomes]
rs61455710	1.00[AMR][1000 genomes]
rs6768539	1.00[AMR][1000 genomes]
rs6789552	1.00[AMR][1000 genomes]
rs73833231	1.00[AMR][1000 genomes]
rs73833232	1.00[AMR][1000 genomes]
rs73833239	1.00[AMR][1000 genomes]
rs73833242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833247	1.00[AMR][1000 genomes]
rs73833404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833886	1.00[AMR][1000 genomes]
rs73833935	1.00[AMR][1000 genomes]
rs73833940	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833943	1.00[AMR][1000 genomes]
rs73833947	1.00[AMR][1000 genomes]
rs73833949	1.00[AMR][1000 genomes]
rs73833952	1.00[AMR][1000 genomes]
rs73833954	1.00[AMR][1000 genomes]
rs73835533	1.00[AMR][1000 genomes]
rs73835535	1.00[AMR][1000 genomes]
rs73835537	1.00[AMR][1000 genomes]
rs73835538	1.00[AMR][1000 genomes]
rs7642578	1.00[AMR][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	nsv967016	chr3:50753594-50759813	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50759000-50759800	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr3:50759000-50759800	Enhancers	Brain Hippocampus Middle	brain
3	chr3:50759200-50759800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:50759400-50759600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:50759400-50759800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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