Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10128512	0.83[YRI][hapmap]
rs10828918	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs10828930	1.00[ASW][hapmap];0.94[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs11014881	0.84[AFR][1000 genomes]
rs11014916	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014926	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014941	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014956	1.00[AMR][1000 genomes]
rs11498425	1.00[AMR][1000 genomes]
rs11814511	1.00[ASW][hapmap];0.87[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs11814982	0.93[AFR][1000 genomes]
rs11819023	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs12241145	0.90[YRI][hapmap]
rs12247532	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs12249093	0.83[YRI][hapmap]
rs12250247	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12260381	0.82[AFR][1000 genomes]
rs12261092	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12263784	0.83[AFR][1000 genomes]
rs12264399	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12265482	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12268743	1.00[AMR][1000 genomes]
rs12385769	1.00[AMR][1000 genomes]
rs7085644	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7098026	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7896360	1.00[ASW][hapmap];0.94[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs7905635	0.83[YRI][hapmap]

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	nsv894974	chr10:26028530-26322783	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv1792417	chr10:26263695-26395038	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26304000-26313200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26306000-26313600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr10:26306000-26314200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr10:26306200-26314600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr10:26310200-26313800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:26310600-26314600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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