Variant report

Variant	rs28516651
Chromosome Location	chr4:86941469-86941470
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10002407	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10027225	0.83[ASN][1000 genomes]
rs10031752	0.92[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs11929863	0.95[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1201	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs13103374	0.86[ASN][1000 genomes]
rs13353771	0.96[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1469869	0.82[ASN][1000 genomes]
rs1898248	0.83[ASN][1000 genomes]
rs1898249	0.90[ASN][1000 genomes]
rs1946733	0.95[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2118044	0.82[ASN][1000 genomes]
rs2282596	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2282597	0.96[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2282598	0.96[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2589506	0.88[ASN][1000 genomes]
rs2589515	0.88[ASN][1000 genomes]
rs2589516	0.88[ASN][1000 genomes]
rs28485608	0.82[ASN][1000 genomes]
rs28865277	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34998174	0.83[ASN][1000 genomes]
rs35823399	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs3755970	0.83[AFR][1000 genomes]
rs3775167	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3775170	0.96[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs3775184	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6840318	0.82[ASN][1000 genomes]
rs9307015	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs958	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9884282	0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009622	chr4:86893536-87119153	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86916800-86985400	Weak transcription	Ovary	ovary
2	chr4:86917000-86954000	Weak transcription	Pancreas	Pancrea
3	chr4:86928600-86953400	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:86932800-86953800	Weak transcription	Fetal Lung	lung
5	chr4:86934200-86942200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:86934200-86953400	Weak transcription	Aorta	Aorta
7	chr4:86935200-86942200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:86935200-86949200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:86936000-86948000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr4:86936000-86975600	Weak transcription	Brain Germinal Matrix	brain
11	chr4:86936400-86954600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr4:86936400-86990600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:86936600-86948000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:86936800-86953600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr4:86938200-86954200	Weak transcription	Fetal Kidney	kidney
16	chr4:86938400-86953400	Weak transcription	Brain Hippocampus Middle	brain
17	chr4:86938600-86945800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr4:86938600-86949000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr4:86938600-86953400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr4:86938600-86953600	Weak transcription	Brain Angular Gyrus	brain
21	chr4:86938600-86954000	Weak transcription	Brain Cingulate Gyrus	brain
22	chr4:86938600-86957800	Weak transcription	Fetal Brain Female	brain
23	chr4:86939200-86953800	Weak transcription	Fetal Stomach	stomach
24	chr4:86941200-86942200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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