Variant report

Variant	rs12586637
Chromosome Location	chr14:84330614-84330615
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10137336	0.93[ASN][1000 genomes]
rs10146014	0.98[ASN][1000 genomes]
rs10149682	0.93[ASN][1000 genomes]
rs10149704	0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10150517	0.91[ASN][1000 genomes]
rs10484118	0.84[EUR][1000 genomes]
rs12588002	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1511318	0.89[ASN][1000 genomes]
rs1698258	0.87[ASN][1000 genomes]
rs1705662	0.85[ASN][1000 genomes]
rs17119147	0.93[ASN][1000 genomes]
rs17119189	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17637116	0.84[ASN][1000 genomes]
rs17643817	0.98[ASN][1000 genomes]
rs17644913	0.84[EUR][1000 genomes]
rs17644974	0.84[EUR][1000 genomes]
rs17645053	0.84[EUR][1000 genomes]
rs17710375	0.89[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs17711443	0.98[ASN][1000 genomes]
rs17711598	0.98[ASN][1000 genomes]
rs17712343	0.84[EUR][1000 genomes]
rs17712396	0.84[EUR][1000 genomes]
rs2026205	0.89[EUR][1000 genomes]
rs2026206	0.89[EUR][1000 genomes]
rs2026207	0.88[EUR][1000 genomes]
rs28693875	0.93[ASN][1000 genomes]
rs55959064	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57002888	0.87[ASN][1000 genomes]
rs59712100	0.89[ASN][1000 genomes]
rs7145520	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7156850	0.96[ASN][1000 genomes]
rs72697170	0.82[EUR][1000 genomes]
rs72697171	0.87[ASN][1000 genomes]
rs72697173	0.87[ASN][1000 genomes]
rs72697185	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8003162	0.89[ASN][1000 genomes]
rs8003919	0.93[ASN][1000 genomes]
rs9323741	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751287	chr14:84294487-84338247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv565375	chr14:84299666-84336944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1054166	chr14:84299761-84338200	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1036610	chr14:84299761-84338626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1051093	chr14:84303380-84338626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv431019	chr14:84303525-84365447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv520014	chr14:84311967-84336944	Enhancers Flanking Active TSS Weak transcription	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	chr14:84329800-84331000	Enhancers	Fetal Stomach	stomach
2	chr14:84329800-84331200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr14:84330000-84336200	Weak transcription	Fetal Brain Female	brain
4	chr14:84330400-84332200	Enhancers	Fetal Brain Male	brain
5	chr14:84330400-84333800	Weak transcription	Ovary	ovary
6	chr14:84330600-84331000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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