Variant report

Variant	rs13389363
Chromosome Location	chr2:62726509-62726510
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	chr2:62724451..62726698-chr2:62729521..62731262,2	MCF-7	breast:
2	chr2:62726106..62729574-chr2:62730789..62734406,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000186889	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10191324	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10191428	0.95[AFR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11125927	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11903221	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13035295	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13388903	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13396048	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4286259	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4405748	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4672527	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4672528	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57645001	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6745280	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6757222	0.93[ASN][1000 genomes]
rs6757448	0.93[ASN][1000 genomes]
rs73934251	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73934252	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73934253	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7582882	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7604354	0.93[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	nsv535766	chr2:62177655-62929746	Bivalent/Poised TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv916190	chr2:62233785-63006200	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv932487	chr2:62258290-63006200	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv535767	chr2:62461582-63413596	Bivalent Enhancer Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv2751	chr2:62691264-62737131	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:62705800-62732200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:62706600-62726600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:62713400-62732400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:62714000-62728000	Weak transcription	Brain Anterior Caudate	brain
5	chr2:62714200-62732400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:62714400-62728400	Weak transcription	HMEC	breast
7	chr2:62716600-62728200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr2:62716600-62732200	Weak transcription	Brain Angular Gyrus	brain
9	chr2:62716600-62732400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr2:62716800-62732000	Weak transcription	Brain Hippocampus Middle	brain
11	chr2:62717200-62728800	Weak transcription	NHDF-Ad	bronchial
12	chr2:62717600-62732400	Weak transcription	Fetal Muscle Leg	muscle
13	chr2:62717600-62732600	Weak transcription	Ovary	ovary
14	chr2:62719600-62732800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:62722600-62728800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:62723000-62732200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:62723200-62728400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:62723600-62728200	Weak transcription	A549	lung
19	chr2:62723600-62728600	Weak transcription	Adipose Nuclei	Adipose
20	chr2:62723600-62728800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:62723600-62732200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:62724600-62728200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr2:62725000-62728000	Weak transcription	HepG2	liver
24	chr2:62725000-62732000	Weak transcription	Fetal Intestine Large	intestine
25	chr2:62725000-62732400	Weak transcription	Fetal Lung	lung
26	chr2:62725200-62726600	Weak transcription	K562	blood
27	chr2:62725200-62728000	Weak transcription	Fetal Intestine Small	intestine
28	chr2:62725200-62728800	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr2:62725200-62732200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr2:62725800-62728200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:62726200-62726800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:62726200-62727200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:62726200-62727200	Enhancers	Osteobl	bone
34	chr2:62726200-62727400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:62726200-62727400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:62726400-62728400	Weak transcription	Fetal Brain Female	brain
37	chr2:62726400-62732400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:62726400-62732400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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