Variant report

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11916346	0.85[AFR][1000 genomes]
rs11917290	0.82[YRI][hapmap];0.85[AFR][1000 genomes]
rs11919150	0.85[AFR][1000 genomes]
rs11921571	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11923981	0.82[AFR][1000 genomes]
rs11926441	1.00[AMR][1000 genomes]
rs11928996	0.88[AFR][1000 genomes]
rs17005793	1.00[AMR][1000 genomes]
rs17005804	1.00[AMR][1000 genomes]
rs17005815	0.88[AFR][1000 genomes]
rs17005821	0.85[AFR][1000 genomes]
rs17005825	1.00[AMR][1000 genomes]
rs17005826	0.83[YRI][hapmap];0.85[AFR][1000 genomes]
rs17005829	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17005831	0.83[YRI][hapmap];0.85[AFR][1000 genomes]
rs17005837	0.83[YRI][hapmap];0.82[AFR][1000 genomes]
rs17005844	0.81[AFR][1000 genomes]
rs17005849	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17006074	1.00[MEX][hapmap]
rs17043802	1.00[AMR][1000 genomes]
rs72937857	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937861	0.82[AFR][1000 genomes]
rs72937877	0.85[AFR][1000 genomes]
rs72937880	0.82[AFR][1000 genomes]
rs72937883	0.85[AFR][1000 genomes]
rs72937885	0.85[AFR][1000 genomes]
rs72937887	0.88[AFR][1000 genomes]
rs72937889	0.88[AFR][1000 genomes]
rs72937895	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937901	0.84[AFR][1000 genomes]
rs72937902	0.85[AFR][1000 genomes]
rs72939655	0.93[AFR][1000 genomes]
rs72939706	0.85[AFR][1000 genomes]
rs72939709	0.85[AFR][1000 genomes]
rs72939711	0.85[AFR][1000 genomes]
rs72939718	0.85[AFR][1000 genomes]
rs72939723	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007730	chr3:69355932-69730587	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2760780	chr3:69413876-69513947	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3426797	chr3:69433086-69777229	Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69439000-69449600	Weak transcription	Fetal Lung	lung
2	chr3:69440000-69453800	Weak transcription	HMEC	breast
3	chr3:69441800-69450000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:69446600-69448000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:69446600-69452600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:69446600-69452800	Weak transcription	NHEK	skin
7	chr3:69447600-69448000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:69447600-69448200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr3:69447600-69448600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr3:69447600-69453400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:69447800-69448000	Enhancers	Brain Substantia Nigra	brain
12	chr3:69447800-69448600	Enhancers	Brain Inferior Temporal Lobe	brain

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