Variant report

Variant	rs1535766
Chromosome Location	chr9:110012041-110012042
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:110000595..110013733-chr9:110042800..110048700,27	MCF-7	breast:
2	chr9:110007992..110013194-chr9:110021107..110025881,5	MCF-7	breast:
3	chr9:110009648..110012591-chr9:110013011..110015349,2	K562	blood:
4	chr9:110011669..110017049-chr9:110043880..110047775,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000119318	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10113916	0.89[CHB][hapmap]
rs10119641	0.89[CHB][hapmap]
rs10481632	0.89[CHB][hapmap]
rs10521083	0.83[CHB][hapmap]
rs10732368	0.83[CHB][hapmap]
rs10739232	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10739234	0.83[CHB][hapmap]
rs10739238	0.83[CHB][hapmap]
rs10759218	0.88[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10759219	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap];1.00[ASN][1000 genomes]
rs10759220	1.00[ASN][1000 genomes]
rs10759221	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10759222	0.83[CHB][hapmap]
rs10759225	0.89[CHB][hapmap]
rs10816471	0.92[ASN][1000 genomes]
rs10816472	0.80[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.95[MKK][hapmap];0.92[ASN][1000 genomes]
rs10816473	0.83[ASN][1000 genomes]
rs10816474	0.83[ASN][1000 genomes]
rs10816475	0.89[CHB][hapmap];0.87[EUR][1000 genomes]
rs10816477	0.89[CHB][hapmap]
rs10816485	0.89[CHB][hapmap]
rs10816492	0.89[CHB][hapmap]
rs10978764	0.80[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.92[ASN][1000 genomes]
rs10978765	0.92[ASN][1000 genomes]
rs10978766	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10978767	0.94[CHB][hapmap];0.94[CHD][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs10978769	0.89[CHB][hapmap];0.91[CHD][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs10978770	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10978775	0.89[CHB][hapmap]
rs10978791	0.89[CHB][hapmap]
rs12345455	0.89[CHB][hapmap]
rs1323806	0.85[CHB][hapmap];0.89[CHD][hapmap]
rs1323808	0.83[CHB][hapmap]
rs1323809	0.89[CHB][hapmap]
rs1408135	0.89[CHB][hapmap]
rs1519051	0.92[ASN][1000 genomes]
rs1519052	0.92[ASN][1000 genomes]
rs1535765	0.83[CHB][hapmap]
rs1535767	0.92[ASN][1000 genomes]
rs1805329	0.89[CHB][hapmap]
rs1805332	0.83[CHB][hapmap]
rs1805334	0.83[CHB][hapmap]
rs1886134	0.83[CHB][hapmap]
rs2015605	0.82[ASN][1000 genomes]
rs2147072	0.83[CHB][hapmap]
rs2417784	0.89[CHB][hapmap]
rs2417785	0.83[CHB][hapmap]
rs2680218	0.92[ASN][1000 genomes]
rs2680219	0.92[ASN][1000 genomes]
rs2808364	0.92[ASN][1000 genomes]
rs4278207	0.83[CHB][hapmap]
rs4481670	0.83[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4978764	0.89[CHB][hapmap]
rs4978849	0.83[CHB][hapmap]
rs698475	0.89[CHB][hapmap]
rs7029997	0.83[CHB][hapmap]
rs7030169	0.83[CHB][hapmap]
rs7031906	0.83[CHB][hapmap]
rs7035611	0.83[CHB][hapmap]
rs7038737	0.82[CHB][hapmap]
rs7041137	0.88[CHB][hapmap]
rs7041497	0.83[CHB][hapmap]
rs7046950	0.83[CHB][hapmap]
rs7847661	0.92[ASN][1000 genomes]
rs7847784	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7848194	0.92[CEU][hapmap];0.80[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.87[MKK][hapmap];0.87[TSI][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7852259	0.80[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7852295	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.94[MKK][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7861304	0.83[ASN][1000 genomes]
rs7861645	0.80[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7861827	0.92[ASN][1000 genomes]
rs7862063	0.95[JPT][hapmap]
rs7862103	0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7866312	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[MKK][hapmap];1.00[ASN][1000 genomes]
rs7866353	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7866797	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[MKK][hapmap];1.00[ASN][1000 genomes]
rs7867544	0.94[CHB][hapmap];0.82[CHD][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs7867706	0.80[AFR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7873081	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs817836	0.89[CHB][hapmap]
rs817840	0.89[CHB][hapmap]
rs817841	0.89[CHB][hapmap]
rs942291	0.89[CHB][hapmap]
rs942293	0.83[CHB][hapmap]
rs9632893	0.83[CHB][hapmap]
rs9969728	0.89[CHB][hapmap]

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	nsv869351	chr9:109593212-110191170	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv831682	chr9:109937181-110075453	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv893698	chr9:109998563-110052660	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv508560	chr9:110006490-110060539	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110006600-110013000	Enhancers	Placenta	Placenta
2	chr9:110006600-110013600	Weak transcription	NH-A	brain
3	chr9:110006800-110012200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:110007000-110022600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr9:110008800-110014200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:110008800-110014400	Weak transcription	Fetal Kidney	kidney
7	chr9:110009800-110015400	Enhancers	Fetal Muscle Leg	muscle
8	chr9:110010000-110012400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:110010000-110012400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:110010000-110012400	Enhancers	Pancreas	Pancrea
11	chr9:110010000-110014200	Enhancers	HSMMtube	muscle
12	chr9:110010200-110012400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr9:110010400-110013000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:110010600-110012400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:110010600-110013600	Weak transcription	Psoas Muscle	Psoas
16	chr9:110010800-110012400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:110011000-110012200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:110011000-110012200	Flanking Active TSS	A549	lung
19	chr9:110011000-110012400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:110011000-110012400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr9:110011000-110012400	Enhancers	HSMM	muscle
22	chr9:110011000-110012400	Enhancers	Osteobl	bone
23	chr9:110011000-110012600	Enhancers	NHLF	lung
24	chr9:110011200-110012200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:110011200-110012200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr9:110011200-110012400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:110011200-110012400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:110011200-110013800	Enhancers	NHDF-Ad	bronchial
29	chr9:110011200-110014200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:110011400-110012200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr9:110011400-110012400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr9:110011400-110012600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:110011400-110014600	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr9:110011600-110012200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:110011600-110012400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr9:110011600-110012400	Enhancers	Liver	Liver
37	chr9:110011800-110012400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:110011800-110012400	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr9:110011800-110012400	Enhancers	HMEC	breast
40	chr9:110011800-110012600	Enhancers	NHEK	skin
41	chr9:110011800-110013600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr9:110011800-110013600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:110011800-110013600	Weak transcription	Ovary	ovary
44	chr9:110011800-110013800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:110011800-110013800	Weak transcription	Adipose Nuclei	Adipose
46	chr9:110011800-110014200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr9:110012000-110012200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr9:110012000-110013600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:110012000-110014200	Enhancers	HepG2	liver

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