Variant report

Variant	rs11802598
Chromosome Location	chr1:216960260-216960261
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11800710	1.00[AMR][1000 genomes]
rs11809093	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11809114	0.80[YRI][hapmap];0.82[AFR][1000 genomes]
rs17043841	0.82[YRI][hapmap];0.85[AFR][1000 genomes]
rs61094558	0.85[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	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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216958800-216963600	Weak transcription	Fetal Brain Male	brain
2	chr1:216958800-216967400	Weak transcription	Right Atrium	heart
3	chr1:216959400-216963000	Weak transcription	Left Ventricle	heart
4	chr1:216959400-216964600	Weak transcription	Pancreas	Pancrea
5	chr1:216960000-216962600	Weak transcription	Fetal Heart	heart

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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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