Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11159350	1.00[CHB][hapmap]
rs11159352	1.00[CHB][hapmap]
rs12880553	1.00[CHB][hapmap]
rs13329054	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1523131	1.00[CHB][hapmap]
rs1882811	1.00[CHB][hapmap]
rs1882812	1.00[CHB][hapmap]
rs2205163	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2205164	1.00[CHB][hapmap]
rs4503718	1.00[CHB][hapmap]
rs4903742	1.00[CHB][hapmap]
rs4903743	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs7140340	1.00[CHB][hapmap]
rs7144427	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7148087	1.00[CHB][hapmap]
rs7149016	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7152608	0.85[YRI][hapmap]
rs8018121	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8018257	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8021038	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs986980	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][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	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1054051	chr14:78772614-78805311	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78738600-78778200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:78738600-78779000	Weak transcription	Brain Angular Gyrus	brain
3	chr14:78750200-78778400	Weak transcription	Brain Anterior Caudate	brain
4	chr14:78769200-78783200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:78774600-78782600	Weak transcription	Fetal Brain Male	brain
6	chr14:78774800-78778200	Weak transcription	Fetal Kidney	kidney
7	chr14:78774800-78778200	Weak transcription	Fetal Lung	lung
8	chr14:78775200-78778600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:78775400-78777800	Enhancers	Brain Germinal Matrix	brain

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