Variant report

Variant	rs56347716
Chromosome Location	chr7:48721651-48721652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11771415	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12672686	0.87[AMR][1000 genomes]
rs34725076	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4917167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55744251	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48720600-48723200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr7:48721400-48722600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:48721600-48722000	Enhancers	Brain Cingulate Gyrus	brain
4	chr7:48721600-48722800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:48721600-48722800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:48721600-48723200	Enhancers	Brain Substantia Nigra	brain

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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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