Variant report

Variant	rs61064771
Chromosome Location	chr10:117688812-117688813
allele	C/T
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:16)

rs_ID	r²[population]
rs10490986	0.86[AFR][1000 genomes]
rs10490987	0.86[AFR][1000 genomes]
rs17093832	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2615878	1.00[EUR][1000 genomes]
rs55782493	0.86[AFR][1000 genomes]
rs55917752	0.86[AFR][1000 genomes]
rs56756071	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57211763	0.86[AFR][1000 genomes]
rs58744761	0.86[AFR][1000 genomes]
rs61170750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67778998	0.86[AFR][1000 genomes]
rs73365746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73365748	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73365760	0.86[AFR][1000 genomes]
rs73365779	1.00[EUR][1000 genomes]
rs74160725	1.00[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117658200-117695400	Weak transcription	Aorta	Aorta
2	chr10:117679000-117692800	Weak transcription	HSMM	muscle

Quick Search:

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

what's new

Quick links