Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10265163	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17132372	1.00[CEU][hapmap]
rs17132432	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs17132434	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs17132444	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs17132457	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs17132463	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs17132508	0.85[CEU][hapmap];1.00[EUR][1000 genomes]
rs41356045	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap]
rs41523451	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs55651521	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59965341	0.85[EUR][1000 genomes]
rs6951282	1.00[CEU][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs6971823	0.85[EUR][1000 genomes]
rs73324228	0.85[EUR][1000 genomes]
rs73324231	0.90[EUR][1000 genomes]
rs73694659	0.85[EUR][1000 genomes]
rs73694660	0.85[EUR][1000 genomes]
rs73694665	0.85[EUR][1000 genomes]
rs73694667	0.85[EUR][1000 genomes]
rs73694668	0.85[EUR][1000 genomes]
rs73694670	0.85[EUR][1000 genomes]
rs73694671	0.85[EUR][1000 genomes]
rs73694678	0.85[EUR][1000 genomes]
rs73694693	0.95[EUR][1000 genomes]
rs73694694	1.00[EUR][1000 genomes]
rs73694695	1.00[EUR][1000 genomes]
rs7793028	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7801591	0.82[CEU][hapmap];1.00[EUR][1000 genomes]
rs7812121	1.00[EUR][1000 genomes]
rs9969343	1.00[CEU][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830992	chr7:48497408-48686442	Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv606894	chr7:48663637-48718598	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48672400-48683000	Weak transcription	Fetal Lung	lung
2	chr7:48672600-48688800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:48676800-48683200	Weak transcription	Right Atrium	heart
4	chr7:48677600-48682600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:48677800-48682400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr7:48679200-48682200	Weak transcription	Right Ventricle	heart
7	chr7:48679200-48683400	Weak transcription	Left Ventricle	heart
8	chr7:48681000-48682600	Enhancers	Fetal Heart	heart
9	chr7:48682000-48682800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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