Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10137336	0.96[ASN][1000 genomes]
rs10146014	0.95[ASN][1000 genomes]
rs10149682	0.96[ASN][1000 genomes]
rs10149704	0.89[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10150517	0.94[ASN][1000 genomes]
rs12586637	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12588002	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1511318	0.87[ASN][1000 genomes]
rs1698258	0.85[ASN][1000 genomes]
rs1705662	0.83[ASN][1000 genomes]
rs17119147	0.96[ASN][1000 genomes]
rs17637116	0.82[ASN][1000 genomes]
rs17643817	0.95[ASN][1000 genomes]
rs17710375	0.89[CHB][hapmap];0.87[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17711443	0.95[ASN][1000 genomes]
rs17711598	0.95[ASN][1000 genomes]
rs2026205	0.81[EUR][1000 genomes]
rs2026206	0.81[EUR][1000 genomes]
rs2026207	0.81[EUR][1000 genomes]
rs28693875	0.91[ASN][1000 genomes]
rs55959064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57002888	0.85[ASN][1000 genomes]
rs59712100	0.87[ASN][1000 genomes]
rs7145520	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7156850	0.98[ASN][1000 genomes]
rs72697171	0.85[ASN][1000 genomes]
rs72697173	0.85[ASN][1000 genomes]
rs72697185	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8003162	0.87[ASN][1000 genomes]
rs8003919	0.91[ASN][1000 genomes]
rs9323741	0.91[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	nsv431019	chr14:84303525-84365447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv902159	chr14:84336944-84447356	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84337000-84342400	Enhancers	Fetal Stomach	stomach
2	chr14:84338400-84340600	Weak transcription	HSMMtube	muscle
3	chr14:84339800-84340200	Enhancers	Colon Smooth Muscle	Colon
4	chr14:84339800-84340200	Enhancers	Rectal Smooth Muscle	rectum
5	chr14:84339800-84340400	Enhancers	Fetal Lung	lung
6	chr14:84339800-84340600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:84339800-84341200	Enhancers	Fetal Kidney	kidney
8	chr14:84340000-84342600	Weak transcription	Ovary	ovary

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