Variant report

Variant	rs9822445
Chromosome Location	chr3:116161534-116161535
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10804523	0.95[CEU][hapmap]
rs1367772	0.89[CEU][hapmap]
rs1623237	0.86[CEU][hapmap]
rs16824930	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1713005	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1731607	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1795283	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1920064	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1920184	0.95[CEU][hapmap]
rs1920190	0.95[CEU][hapmap]
rs1920192	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2033406	0.95[CEU][hapmap]
rs34073129	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4831131	0.95[CEU][hapmap]
rs6783360	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9823782	0.95[CEU][hapmap]
rs9838639	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9869410	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9870357	0.95[CEU][hapmap]

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	esv2757886	chr3:116142130-116307542	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2759171	chr3:116142130-116307542	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116158400-116161800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:116158800-116161600	Enhancers	NH-A	brain
3	chr3:116159000-116163400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:116160200-116162200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:116160400-116165000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr3:116160600-116165200	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr3:116160800-116162600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:116160800-116164600	Active TSS	Brain Hippocampus Middle	brain
9	chr3:116161000-116161600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:116161000-116161600	Enhancers	Fetal Stomach	stomach
11	chr3:116161000-116163200	Active TSS	Stomach Smooth Muscle	stomach
12	chr3:116161000-116164000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:116161000-116164600	Active TSS	Rectal Smooth Muscle	rectum
14	chr3:116161000-116164800	Active TSS	Fetal Brain Female	brain
15	chr3:116161000-116165200	Active TSS	Brain Substantia Nigra	brain
16	chr3:116161200-116161600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr3:116161200-116161600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:116161200-116161600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr3:116161200-116161600	Flanking Active TSS	Fetal Brain Male	brain
20	chr3:116161200-116161600	Flanking Bivalent TSS/Enh	Fetal Lung	lung
21	chr3:116161200-116161800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:116161200-116161800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr3:116161200-116161800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:116161200-116161800	Active TSS	Brain Cingulate Gyrus	brain
25	chr3:116161200-116161800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr3:116161200-116162000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr3:116161200-116162000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:116161200-116162000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr3:116161200-116162000	Enhancers	Fetal Kidney	kidney
30	chr3:116161200-116162200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr3:116161200-116162200	Weak transcription	Fetal Muscle Trunk	muscle
32	chr3:116161200-116163000	Active TSS	Brain Anterior Caudate	brain
33	chr3:116161200-116164600	Active TSS	Brain Angular Gyrus	brain
34	chr3:116161200-116164600	Active TSS	Colon Smooth Muscle	Colon
35	chr3:116161400-116162000	Weak transcription	Fetal Intestine Large	intestine
36	chr3:116161400-116162200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr3:116161400-116162200	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr3:116161400-116162400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr3:116161400-116162600	Active TSS	Brain Germinal Matrix	brain
40	chr3:116161400-116163200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr3:116161400-116164400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr3:116161400-116164600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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