Variant report

Variant	rs7522593
Chromosome Location	chr1:216958033-216958034
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10218498	0.82[GIH][hapmap]
rs11117675	0.86[GIH][hapmap]
rs12023645	0.88[CHD][hapmap]
rs12048695	0.86[GIH][hapmap]
rs1572738	0.86[GIH][hapmap]
rs9970445	0.86[GIH][hapmap]

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	esv2762162	chr1:216942781-216966140	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216897400-216958600	Weak transcription	Pancreas	Pancrea
2	chr1:216939800-216958600	Weak transcription	Psoas Muscle	Psoas
3	chr1:216952000-216958600	Weak transcription	Aorta	Aorta
4	chr1:216953400-216958600	Weak transcription	Fetal Heart	heart
5	chr1:216955000-216958800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:216955600-216958600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:216957600-216958600	Weak transcription	Right Atrium	heart
8	chr1:216957800-216958600	Enhancers	Fetal Lung	lung
9	chr1:216958000-216958400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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