Variant report

Variant	rs1494225
Chromosome Location	chr3:22466842-22466843
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1121249	0.95[CHD][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs13079500	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs13100427	0.85[ASN][1000 genomes]
rs1349271	1.00[YRI][hapmap]
rs1376036	0.84[ASW][hapmap];1.00[YRI][hapmap]
rs1389664	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs1603022	0.91[JPT][hapmap]
rs1603023	0.95[CHD][hapmap];0.91[JPT][hapmap]
rs1817029	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1947238	1.00[YRI][hapmap]
rs1966824	0.87[CEU][hapmap];0.87[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.86[TSI][hapmap]
rs1975628	0.84[ASW][hapmap]
rs35821736	0.85[ASN][1000 genomes]
rs4858402	0.84[CHD][hapmap];0.91[JPT][hapmap]
rs6778816	0.90[JPT][hapmap]
rs903289	0.82[JPT][hapmap]
rs935736	0.91[JPT][hapmap]
rs982355	0.93[CHD][hapmap];0.86[JPT][hapmap]
rs9863827	0.86[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003211	chr3:22244883-22584229	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv536520	chr3:22244883-22584229	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv428082	chr3:22397625-22539817	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv834634	chr3:22420053-22574021	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1494225	CYP1B1	trans	lymphoblastoid	seeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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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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