Variant report

Variant	rs914928
Chromosome Location	chr9:93624755-93624756
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	chr9:93562955..93565844-chr9:93624678..93627429,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165025	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1760124	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1760125	1.00[ASN][1000 genomes]
rs2613310	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs290203	0.94[ASN][1000 genomes]
rs290204	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs290225	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs290256	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs290257	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2991216	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs914929	1.00[ASN][1000 genomes]
rs965892	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv831652	chr9:93527411-93696923	Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1038685	chr9:93556174-93685729	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1039761	chr9:93598856-93677831	Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1039326	chr9:93598856-93685729	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv430078	chr9:93609668-93642766	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1053252	chr9:93610132-93699103	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv430079	chr9:93620963-93642766	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93601800-93642200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:93605000-93633000	Weak transcription	Fetal Kidney	kidney
3	chr9:93605800-93631000	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr9:93611200-93642200	Weak transcription	Stomach Mucosa	stomach
5	chr9:93617200-93640600	Weak transcription	K562	blood
6	chr9:93617400-93629600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:93617400-93640600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:93617800-93640600	Weak transcription	NHEK	skin
9	chr9:93619400-93630000	Strong transcription	Thymus	Thymus
10	chr9:93619800-93627000	Strong transcription	Fetal Intestine Small	intestine
11	chr9:93620800-93625600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr9:93621200-93626600	Strong transcription	Fetal Thymus	thymus
13	chr9:93621200-93631400	Strong transcription	Primary B cells from cord blood	blood
14	chr9:93621600-93626200	Weak transcription	Primary T cells from cord blood	blood
15	chr9:93622400-93629200	Weak transcription	Pancreas	Pancrea
16	chr9:93622600-93631200	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr9:93622800-93630000	Strong transcription	Fetal Stomach	stomach
18	chr9:93623000-93626400	Weak transcription	Small Intestine	intestine
19	chr9:93623200-93625800	Strong transcription	Esophagus	oesophagus
20	chr9:93623200-93626000	Strong transcription	Primary hematopoietic stem cells	blood
21	chr9:93623200-93626200	Strong transcription	Colonic Mucosa	Colon
22	chr9:93623200-93626800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:93623200-93630000	Strong transcription	Duodenum Mucosa	Duodenum
24	chr9:93623200-93630800	Strong transcription	GM12878-XiMat	blood
25	chr9:93623400-93625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:93623400-93627000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr9:93623600-93627400	Strong transcription	Spleen	Spleen
28	chr9:93623600-93627800	Strong transcription	Rectal Mucosa Donor 31	rectum
29	chr9:93623600-93631200	Strong transcription	Primary B cells from peripheral blood	blood
30	chr9:93623600-93642400	Weak transcription	Adipose Nuclei	Adipose
31	chr9:93623800-93626800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr9:93623800-93630400	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr9:93623800-93631000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr9:93623800-93631400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr9:93624000-93625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:93624000-93625600	Strong transcription	Gastric	stomach
37	chr9:93624000-93630000	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr9:93624000-93631200	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr9:93624200-93630000	Strong transcription	Fetal Intestine Large	intestine
40	chr9:93624400-93625000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:93624400-93625600	Strong transcription	Lung	lung
42	chr9:93624600-93625000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:93624600-93626000	Strong transcription	Duodenum Smooth Muscle	Duodenum

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