Variant report

Variant	rs72815929
Chromosome Location	chr5:114652296-114652297
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17137632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2605174	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs267284	0.89[EUR][1000 genomes]
rs2925174	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56385991	1.00[ASN][1000 genomes]
rs72813858	1.00[ASN][1000 genomes]
rs72815919	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72815924	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72815926	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72815932	0.93[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114651400-114652400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr5:114651800-114652400	Enhancers	Brain Hippocampus Middle	brain
3	chr5:114652200-114652400	Enhancers	Left Ventricle	heart

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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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