Variant report

Variant	rs17825737
Chromosome Location	chr4:103369642-103369643
allele	A/G
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:11)

rs_ID	r²[population]
rs11097783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12510679	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12513242	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13115343	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13119968	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13132193	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17825838	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs4699028	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6817730	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6846971	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs926163	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103368400-103370000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:103369000-103373200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr4:103369400-103369800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:103369400-103371000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr4:103369400-103373400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:103369600-103369800	Enhancers	iPS-20b 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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