Variant report

Variant	rs72666116
Chromosome Location	chr14:32792245-32792246
allele	A/C
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]
rs10483399	0.84[EUR][1000 genomes]
rs11623151	0.81[ASN][1000 genomes]
rs17098767	0.81[ASN][1000 genomes]
rs2208868	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3825744	0.95[EUR][1000 genomes]
rs72666119	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72666125	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72666126	1.00[EUR][1000 genomes]
rs72666154	0.86[EUR][1000 genomes]
rs8021139	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32788800-32811800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:32790800-32799800	Weak transcription	Fetal Heart	heart
3	chr14:32791200-32793600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:32791400-32795000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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