Variant report

Variant	rs72777068
Chromosome Location	chr5:91706469-91706470
allele	C/T
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]
rs10041056	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10055515	0.95[EUR][1000 genomes]
rs10055632	0.95[EUR][1000 genomes]
rs10057380	0.83[EUR][1000 genomes]
rs10063190	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10065964	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10073874	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13354246	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777081	0.91[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91706200-91708000	Enhancers	Liver	Liver
2	chr5:91706400-91706800	Enhancers	A549	lung
3	chr5:91706400-91708000	Enhancers	HUES64 Cell Line	embryonic stem cell

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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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