Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12533352	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12536592	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12537147	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12669997	0.91[EUR][1000 genomes]
rs12699654	0.86[EUR][1000 genomes]
rs12699655	0.86[EUR][1000 genomes]
rs12699658	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13231864	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13237347	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1357872	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1525074	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1568846	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17668635	0.86[EUR][1000 genomes]
rs1997040	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34587189	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35046572	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35731392	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4719417	0.88[EUR][1000 genomes]
rs6461121	0.93[EUR][1000 genomes]
rs6965637	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6966274	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71538884	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7785767	0.91[EUR][1000 genomes]
rs9639213	0.91[EUR][1000 genomes]

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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887712	chr7:14717872-14829858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14712800-14775200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:14758800-14763000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:14760200-14760800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr7:14760200-14761200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:14760200-14761800	Enhancers	Colon Smooth Muscle	Colon

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