Variant report

Variant	rs9299090
Chromosome Location	chr9:9264932-9264933
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10116111	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap]
rs10125274	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10816071	0.84[JPT][hapmap]
rs10816075	0.83[JPT][hapmap]
rs10816076	0.84[JPT][hapmap]
rs10977651	0.94[GIH][hapmap]
rs12350625	0.81[CHB][hapmap];0.93[JPT][hapmap]
rs1889105	0.84[JPT][hapmap]
rs4146134	0.93[CHD][hapmap]
rs4146135	0.93[JPT][hapmap]
rs4146136	0.94[GIH][hapmap];0.84[JPT][hapmap]
rs4302899	0.91[GIH][hapmap];0.90[JPT][hapmap]
rs4319157	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs4361814	0.85[CHB][hapmap]
rs4363255	0.85[CHB][hapmap];0.93[CHD][hapmap]
rs4457389	0.84[CHB][hapmap]
rs4492438	0.89[GIH][hapmap]
rs4626664	1.00[CHB][hapmap];0.94[GIH][hapmap];0.95[JPT][hapmap];0.97[LWK][hapmap];1.00[YRI][hapmap]
rs4626665	0.85[CHB][hapmap];0.93[CHD][hapmap];0.84[JPT][hapmap]
rs7872553	0.84[JPT][hapmap]
rs7874373	0.89[JPT][hapmap]
rs9299091	0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498066	chr9:8961722-9486652	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv892249	chr9:9026854-9377679	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv831505	chr9:9072216-9277320	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv892252	chr9:9164473-9476425	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1027042	chr9:9208635-9300048	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	nsv1021440	chr9:9231961-9329870	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
7	nsv892253	chr9:9249912-9287321	Enhancers	n/a	n/a	inside rSNPs	n/a
8	nsv1030899	chr9:9250314-9291197	Enhancers	n/a	n/a	inside rSNPs	n/a
9	nsv892254	chr9:9253587-9348102	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
10	nsv824847	chr9:9255377-9378016	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv613304	chr9:9263980-9295281	Enhancers	n/a	n/a	inside rSNPs	n/a
12	nsv613305	chr9:9263980-9310461	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv1805303	chr9:9264439-9287406	Enhancers	n/a	n/a	inside rSNPs	n/a
14	nsv466129	chr9:9264932-9297697	Enhancers	n/a	n/a	inside rSNPs	n/a
15	nsv892255	chr9:9264932-9348102	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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
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