Variant report

Variant	rs9450796
Chromosome Location	chr6:88462440-88462441
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs9444545	1.00[AFR][1000 genomes]
rs9444546	1.00[AFR][1000 genomes]
rs9444547	1.00[AFR][1000 genomes]
rs9444548	1.00[AFR][1000 genomes]
rs9450789	1.00[AFR][1000 genomes]
rs9450794	1.00[AFR][1000 genomes]
rs9450797	1.00[AFR][1000 genomes]
rs9450798	1.00[AFR][1000 genomes]
rs9450799	1.00[AFR][1000 genomes]
rs9450803	1.00[AFR][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	esv3408957	chr6:88460283-88462481	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:88456400-88465400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:88457800-88482400	Weak transcription	Placenta	Placenta
3	chr6:88458200-88465600	Weak transcription	HepG2	liver
4	chr6:88458400-88464000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr6:88461800-88466000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:88462400-88462800	Enhancers	Monocytes-CD14+_RO01746	blood

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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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