Variant report

Variant	rs962661
Chromosome Location	chr14:82122738-82122739
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10131960	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10143491	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10873339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11844780	0.85[ASN][1000 genomes]
rs12432882	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12589197	1.00[ASN][1000 genomes]
rs12891898	0.84[ASN][1000 genomes]
rs1536711	0.94[ASN][1000 genomes]
rs1536712	0.98[ASN][1000 genomes]
rs17642919	0.85[ASN][1000 genomes]
rs1952368	0.94[ASN][1000 genomes]
rs1957537	0.98[ASN][1000 genomes]
rs1957539	0.99[ASN][1000 genomes]
rs1958206	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1958207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1958208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1958209	1.00[ASN][1000 genomes]
rs1958213	1.00[ASN][1000 genomes]
rs2182974	0.93[ASN][1000 genomes]
rs2209888	0.98[ASN][1000 genomes]
rs2209889	1.00[ASN][1000 genomes]
rs2209890	0.97[ASN][1000 genomes]
rs35078513	0.99[ASN][1000 genomes]
rs35081972	0.94[ASN][1000 genomes]
rs35473249	0.97[ASN][1000 genomes]
rs36092964	0.97[ASN][1000 genomes]
rs3920573	1.00[ASN][1000 genomes]
rs4899790	0.97[ASN][1000 genomes]
rs4904018	1.00[ASN][1000 genomes]
rs6574674	1.00[ASN][1000 genomes]
rs67742323	1.00[ASN][1000 genomes]
rs7143847	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7146268	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7156086	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7157501	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs756019	0.97[ASN][1000 genomes]
rs9323708	1.00[ASN][1000 genomes]
rs962660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9671352	0.97[ASN][1000 genomes]
rs986055	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047694	chr14:81831147-82534026	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv542145	chr14:81831147-82534026	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv565299	chr14:81983027-82586324	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1052666	chr14:82069162-83028382	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv902121	chr14:82075469-82146538	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1375	chr14:82116362-82138158	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:82121800-82122800	Enhancers	Liver	Liver
2	chr14:82121800-82123800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr14:82121800-82124800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:82122000-82122800	Enhancers	Ovary	ovary
5	chr14:82122000-82123000	Enhancers	Adipose Nuclei	Adipose
6	chr14:82122000-82124000	Enhancers	Brain Cingulate Gyrus	brain
7	chr14:82122200-82122800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr14:82122200-82122800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr14:82122200-82122800	Weak transcription	Aorta	Aorta
10	chr14:82122200-82123200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr14:82122200-82123200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr14:82122200-82124600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr14:82122200-82124800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr14:82122400-82122800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:82122400-82123400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr14:82122400-82123600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:82122400-82124600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr14:82122600-82122800	Flanking Active TSS	Brain Anterior Caudate	brain
19	chr14:82122600-82123400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:82122600-82123400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:82122600-82124800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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