Variant report

Variant	rs10178587
Chromosome Location	chr2:10734062-10734063
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:10706246..10708825-chr2:10732569..10734672,2	MCF-7	breast:
2	chr2:10732866..10735426-chr2:10759991..10761967,2	MCF-7	breast:
3	chr2:10724831..10728793-chr2:10731457..10735556,4	MCF-7	breast:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10178751	0.89[AFR][1000 genomes]
rs10183359	0.91[AFR][1000 genomes]
rs10183883	0.86[AFR][1000 genomes]
rs10186984	0.91[AFR][1000 genomes]
rs10207885	0.89[AFR][1000 genomes]
rs10803724	0.91[AFR][1000 genomes]
rs10803725	0.91[AFR][1000 genomes]
rs10929683	0.91[AFR][1000 genomes]
rs10929684	0.91[AFR][1000 genomes]
rs10929685	0.91[AFR][1000 genomes]
rs10929689	0.88[ASN][1000 genomes]
rs11680664	0.86[AFR][1000 genomes]
rs11684537	0.91[AFR][1000 genomes]
rs12104950	0.91[AFR][1000 genomes]
rs12476554	0.91[AFR][1000 genomes]
rs12618726	0.91[AFR][1000 genomes]
rs12690510	0.86[AFR][1000 genomes]
rs12692414	0.86[AFR][1000 genomes]
rs13403486	0.88[ASN][1000 genomes]
rs2024432	0.91[AFR][1000 genomes]
rs2024433	0.88[AFR][1000 genomes]
rs6714787	0.91[AFR][1000 genomes]
rs6740245	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007185	chr2:10540386-10791743	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv833370	chr2:10625149-10785402	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1009897	chr2:10627248-10751468	Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1000953	chr2:10717304-10921805	Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv535584	chr2:10717304-10921805	Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv833381	chr2:10723465-10911284	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10698600-10736600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:10705800-10736000	Strong transcription	Duodenum Mucosa	Duodenum
3	chr2:10709200-10746800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:10712600-10742000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr2:10719800-10746600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr2:10720000-10746400	Strong transcription	Dnd41	blood
7	chr2:10720400-10740200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:10720800-10739200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr2:10721000-10755000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr2:10721200-10734600	Strong transcription	GM12878-XiMat	blood
11	chr2:10721200-10746800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr2:10721400-10735800	Strong transcription	Primary T cells from cord blood	blood
13	chr2:10721600-10735600	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr2:10722000-10735200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:10722000-10738200	Strong transcription	Fetal Muscle Leg	muscle
16	chr2:10722400-10734800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr2:10722400-10735200	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr2:10722800-10741400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:10724000-10735600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr2:10725600-10744000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:10725600-10758800	Weak transcription	Stomach Mucosa	stomach
22	chr2:10725600-10793400	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr2:10725800-10787000	Weak transcription	Fetal Heart	heart
24	chr2:10726000-10738400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:10726000-10746200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr2:10726000-10747600	Strong transcription	HepG2	liver
27	chr2:10727400-10736200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:10727600-10734600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr2:10727600-10737000	Strong transcription	Fetal Intestine Small	intestine
30	chr2:10727600-10739400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:10727800-10735000	Strong transcription	Adipose Nuclei	Adipose
32	chr2:10727800-10740400	Strong transcription	Primary B cells from peripheral blood	blood
33	chr2:10728200-10737800	Weak transcription	NH-A	brain
34	chr2:10728400-10736000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr2:10729200-10738000	Weak transcription	HMEC	breast
36	chr2:10729200-10741600	Weak transcription	Pancreas	Pancrea
37	chr2:10729200-10754200	Weak transcription	NHLF	lung
38	chr2:10729200-10760000	Weak transcription	Brain Angular Gyrus	brain
39	chr2:10729400-10736600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr2:10729400-10740800	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr2:10729400-10741600	Weak transcription	Right Ventricle	heart
42	chr2:10729400-10781800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr2:10729400-10798400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr2:10729600-10734200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:10729600-10736000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:10729600-10736200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:10729600-10738000	Weak transcription	Small Intestine	intestine
48	chr2:10729600-10741400	Weak transcription	Colonic Mucosa	Colon
49	chr2:10729600-10741400	Weak transcription	Spleen	Spleen
50	chr2:10729600-10742000	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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