Variant report

Variant	rs73433504
Chromosome Location	chr15:60033969-60033970
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs16941786	1.00[EUR][1000 genomes]
rs16941800	1.00[EUR][1000 genomes]
rs58234552	1.00[EUR][1000 genomes]
rs58854426	1.00[EUR][1000 genomes]
rs59340067	1.00[EUR][1000 genomes]
rs7171708	1.00[EUR][1000 genomes]
rs7173788	1.00[EUR][1000 genomes]
rs73433557	1.00[EUR][1000 genomes]
rs74018163	1.00[EUR][1000 genomes]
rs74018164	1.00[EUR][1000 genomes]
rs74019636	1.00[EUR][1000 genomes]
rs74019930	1.00[EUR][1000 genomes]
rs74019945	1.00[EUR][1000 genomes]
rs74019947	1.00[EUR][1000 genomes]
rs74019976	1.00[EUR][1000 genomes]
rs8023802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv984219	chr15:60026752-60043941	Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60030000-60034400	Enhancers	Liver	Liver
2	chr15:60033800-60035800	Enhancers	Colon Smooth Muscle	Colon

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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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