Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10132619	0.86[CHB][hapmap]
rs1017186	0.86[CHB][hapmap]
rs1046428	0.86[CHB][hapmap];1.00[YRI][hapmap]
rs11850308	0.86[CHB][hapmap]
rs11850771	0.86[CHB][hapmap]
rs12894594	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12894718	0.86[CHB][hapmap]
rs1468951	0.86[CHB][hapmap]
rs1861888	0.93[CEU][hapmap];1.00[CHB][hapmap]
rs2111700	0.86[CHB][hapmap]
rs2160838	0.86[CHB][hapmap]
rs2270419	0.93[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2363640	0.88[CHB][hapmap]
rs2364155	0.86[CHB][hapmap]
rs3209079	0.93[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3759731	0.86[CHB][hapmap]
rs3815625	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs383064	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4141640	0.93[CEU][hapmap];1.00[CHB][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs451925	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4899649	0.93[CEU][hapmap];0.88[CHB][hapmap]
rs4903566	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs8009177	1.00[YRI][hapmap]
rs9671248	0.86[CHB][hapmap]
rs972725	0.93[CEU][hapmap];0.86[CHB][hapmap];0.80[AMR][1000 genomes];0.81[ASN][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	nsv431017	chr14:76938089-77854647	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv1361	chr14:77707417-77753024	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv902104	chr14:77720741-77756321	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77697600-77726800	Weak transcription	Brain Substantia Nigra	brain
2	chr14:77709800-77729600	Weak transcription	Fetal Brain Male	brain
3	chr14:77711200-77731000	Weak transcription	Spleen	Spleen
4	chr14:77713200-77726800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr14:77718400-77726800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr14:77720800-77726800	Weak transcription	Brain Anterior Caudate	brain
7	chr14:77720800-77727000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr14:77723000-77734000	Weak transcription	Gastric	stomach
9	chr14:77725000-77727000	Weak transcription	Brain Germinal Matrix	brain
10	chr14:77725000-77730400	Weak transcription	Fetal Brain Female	brain
11	chr14:77725600-77727600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:77725800-77726800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:77725800-77727200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:77726000-77727000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr14:77726000-77727600	Weak transcription	Esophagus	oesophagus
16	chr14:77726200-77728000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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