Variant report

Variant	rs11006989
Chromosome Location	chr10:28580992-28580993
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:28551828..28553630-chr10:28580648..28583187,2	MCF-7	breast:
2	chr10:28580079..28588330-chr10:28588541..28593496,9	MCF-7	breast:
3	chr10:28580424..28583414-chr10:28585033..28588040,3	MCF-7	breast:
4	chr10:28580670..28582435-chr10:28590410..28593368,2	MCF-7	breast:
5	chr10:28564267..28567183-chr10:28578724..28581652,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000150054	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10763656	0.87[ASN][1000 genomes]
rs10763657	0.93[ASN][1000 genomes]
rs10826445	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10826446	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006923	0.90[AMR][1000 genomes]
rs11006927	0.86[AMR][1000 genomes]
rs11006928	0.90[AMR][1000 genomes]
rs11006933	0.90[AMR][1000 genomes]
rs11006939	0.86[AMR][1000 genomes]
rs11006947	0.86[AMR][1000 genomes]
rs11006950	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11006954	0.93[AMR][1000 genomes]
rs11006958	0.90[AMR][1000 genomes]
rs11006960	0.93[AMR][1000 genomes]
rs11006990	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11006992	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006994	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11006995	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006997	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs11006998	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006999	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11007000	0.98[AMR][1000 genomes]
rs11007003	0.83[AMR][1000 genomes]
rs11007004	0.81[AMR][1000 genomes]
rs11007006	0.83[AMR][1000 genomes]
rs11007010	0.85[ASN][1000 genomes]
rs12218186	0.82[ASN][1000 genomes]
rs12218294	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12570440	0.95[AMR][1000 genomes]
rs1984853	0.83[AMR][1000 genomes]
rs2368306	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs35016093	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs3842931	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843586	0.86[ASN][1000 genomes]
rs3847386	0.91[ASN][1000 genomes]
rs3847387	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4598572	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4604776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57441879	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7901835	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7902785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7903242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7915405	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7916067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916711	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916740	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv437663	chr10:28562647-28585496	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28550400-28582600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr10:28571400-28584600	Weak transcription	Fetal Intestine Small	intestine
3	chr10:28571600-28583800	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:28571800-28587800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr10:28572400-28582200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:28573600-28581000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr10:28573600-28582600	Weak transcription	Primary T cells from cord blood	blood
8	chr10:28573600-28582600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr10:28573800-28581000	Weak transcription	Fetal Heart	heart
10	chr10:28573800-28587400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr10:28575800-28581000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:28575800-28582000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr10:28576400-28581000	Weak transcription	Colon Smooth Muscle	Colon
14	chr10:28576400-28582200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr10:28577800-28585200	Weak transcription	Gastric	stomach
16	chr10:28578400-28583000	Weak transcription	HepG2	liver
17	chr10:28578600-28583800	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr10:28578800-28582200	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr10:28579000-28588400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr10:28579400-28585000	Weak transcription	Stomach Mucosa	stomach
21	chr10:28580000-28581000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr10:28580000-28581000	Enhancers	NH-A	brain
23	chr10:28580000-28581200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr10:28580000-28581800	Enhancers	HMEC	breast
25	chr10:28580000-28590400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr10:28580200-28581000	Enhancers	Lung	lung
27	chr10:28580200-28581000	Enhancers	Pancreas	Pancrea
28	chr10:28580200-28581200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:28580200-28581200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:28580200-28581200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr10:28580200-28581200	Enhancers	Psoas Muscle	Psoas
32	chr10:28580200-28581200	Enhancers	HSMMtube	muscle
33	chr10:28580200-28581400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:28580200-28581600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:28580200-28581800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr10:28580200-28581800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr10:28580200-28581800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr10:28580200-28581800	Enhancers	NHEK	skin
39	chr10:28580200-28582600	Enhancers	Osteobl	bone
40	chr10:28580200-28582800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr10:28580200-28582800	Enhancers	HSMM	muscle
42	chr10:28580400-28581200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr10:28580400-28581200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr10:28580400-28581400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:28580400-28582200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr10:28580400-28583000	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr10:28580600-28581000	Weak transcription	Aorta	Aorta
48	chr10:28580600-28582400	Weak transcription	Esophagus	oesophagus
49	chr10:28580600-28583800	Weak transcription	Left Ventricle	heart
50	chr10:28580600-28587800	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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