Variant report

Variant	rs4525826
Chromosome Location	chr3:139158078-139158079
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:139156554..139158574-chr3:139162722..139165410,2	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10804665	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1371340	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1599744	1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs167186	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16849065	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849083	1.00[JPT][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176986	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs176988	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs176989	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1873668	0.86[EUR][1000 genomes]
rs211583	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs295491	1.00[JPT][hapmap];0.85[AMR][1000 genomes]
rs4243399	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55735000	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56265838	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60144275	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61525084	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6439851	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6788313	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72988746	0.82[EUR][1000 genomes]
rs7372667	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7372737	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73868351	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7621965	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7636369	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9824044	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9824195	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9838015	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9864352	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9864740	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877543	chr3:139021139-139327261	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1003154	chr3:139060841-139788752	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv536729	chr3:139060841-139788752	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv949635	chr3:139091219-139367043	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	esv2760754	chr3:139144615-139164874	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139136400-139166200	Weak transcription	Fetal Brain Female	brain
2	chr3:139138600-139166200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:139138600-139170400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:139139600-139160000	Weak transcription	Fetal Brain Male	brain
5	chr3:139141200-139160000	Weak transcription	Lung	lung
6	chr3:139141400-139167000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:139142200-139172200	Weak transcription	Fetal Heart	heart
8	chr3:139142600-139158200	Weak transcription	Gastric	stomach
9	chr3:139142800-139162600	Weak transcription	Psoas Muscle	Psoas
10	chr3:139142800-139169000	Weak transcription	Aorta	Aorta
11	chr3:139142800-139176800	Weak transcription	Fetal Stomach	stomach
12	chr3:139144800-139173200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr3:139145200-139158200	Weak transcription	Brain Hippocampus Middle	brain
14	chr3:139145200-139164400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:139145200-139170400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr3:139147200-139158200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr3:139147400-139160200	Weak transcription	Brain Angular Gyrus	brain
18	chr3:139148000-139160000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr3:139149800-139170600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr3:139151800-139158200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:139152200-139159800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:139154000-139167000	Weak transcription	Fetal Muscle Trunk	muscle
23	chr3:139154200-139159200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr3:139154200-139165600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr3:139154200-139168200	Weak transcription	Fetal Intestine Small	intestine
26	chr3:139154200-139171200	Weak transcription	Right Atrium	heart
27	chr3:139154200-139173600	Weak transcription	Ovary	ovary
28	chr3:139154200-139178600	Weak transcription	Left Ventricle	heart
29	chr3:139154400-139159600	Weak transcription	HSMM	muscle
30	chr3:139154400-139166200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr3:139154400-139167000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr3:139154600-139158200	Weak transcription	Adipose Nuclei	Adipose
33	chr3:139154600-139158200	Weak transcription	HSMMtube	muscle
34	chr3:139154800-139165200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr3:139158000-139160800	Enhancers	Brain Substantia Nigra	brain

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