Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17398251	0.83[CEU][hapmap]
rs17398949	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17786463	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1833139	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2109525	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56268815	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61706828	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73101663	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73101665	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73101668	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73101671	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73101690	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73101699	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73103504	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73103508	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73103514	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73103533	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73103557	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7779232	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7793719	1.00[CEU][hapmap];0.85[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv916660	chr7:33272493-33506384	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv830944	chr7:33389892-33549882	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv934287	chr7:33470390-33512880	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv933237	chr7:33470390-33574046	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33475400-33516000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:33493000-33502800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:33493200-33498600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:33493200-33498600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:33493200-33498600	Weak transcription	Osteobl	bone
6	chr7:33496600-33499400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:33496800-33497600	Weak transcription	Fetal Lung	lung

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