Variant report

Variant	rs2906853
Chromosome Location	chr12:68386012-68386013
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs2906854	0.82[AFR][1000 genomes]
rs2906859	0.82[LWK][hapmap];0.94[MKK][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes]
rs2906862	0.85[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3411149	chr12:68066948-68435533	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1039638	chr12:68293351-68399871	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv975509	chr12:68382193-68405026	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2906853	MDM2	cis	parietal	SCAN
rs2906853	FRS2	cis	parietal	SCAN

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:68383800-68386600	Enhancers	Primary T killer memory cells from peripheral blood	blood
2	chr12:68384000-68386800	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr12:68385400-68387000	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr12:68385600-68386200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:68385600-68386400	Enhancers	Primary B cells from cord blood	blood
6	chr12:68385600-68387000	Enhancers	Primary B cells from peripheral blood	blood
7	chr12:68385600-68391000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr12:68385600-68392000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr12:68385800-68386200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr12:68386000-68386200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr12:68386000-68386800	Enhancers	HepG2	liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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