Variant report

Variant	rs36063880
Chromosome Location	chr9:93626609-93626610
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:93563271..93565722-chr9:93625560..93627552,2	MCF-7	breast:
2	chr9:93562955..93565844-chr9:93624678..93627429,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165025	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10124093	0.95[ASN][1000 genomes]
rs10993722	0.84[ASN][1000 genomes]
rs10993723	0.87[ASN][1000 genomes]
rs10993724	0.87[ASN][1000 genomes]
rs10993725	0.87[ASN][1000 genomes]
rs10993727	0.98[ASN][1000 genomes]
rs10993728	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10993729	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12000793	0.97[ASN][1000 genomes]
rs12001366	0.98[ASN][1000 genomes]
rs12003597	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12003608	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12005209	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12005550	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12006330	0.97[ASN][1000 genomes]
rs12686497	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12686499	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1572104	1.00[ASN][1000 genomes]
rs16906904	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16906923	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2290885	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2290886	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2290887	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2290888	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2290890	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2290891	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2306039	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2306041	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34872092	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3789902	0.97[ASN][1000 genomes]
rs3789903	0.97[ASN][1000 genomes]
rs3789905	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3827824	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4529574	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744018	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4744019	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4744516	0.97[ASN][1000 genomes]
rs4744518	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4744519	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55804113	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7020271	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs71494431	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs71494432	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7846754	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7846869	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7866696	0.87[ASN][1000 genomes]
rs7872076	0.95[AMR][1000 genomes];0.98[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:51 , 50 per page) page: 1 2

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	chr9:93621200-93631400	Strong transcription	Primary B cells from cord blood	blood
12	chr9:93622400-93629200	Weak transcription	Pancreas	Pancrea
13	chr9:93622600-93631200	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr9:93622800-93630000	Strong transcription	Fetal Stomach	stomach
15	chr9:93623200-93626800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:93623200-93630000	Strong transcription	Duodenum Mucosa	Duodenum
17	chr9:93623200-93630800	Strong transcription	GM12878-XiMat	blood
18	chr9:93623400-93627000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:93623600-93627400	Strong transcription	Spleen	Spleen
20	chr9:93623600-93627800	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr9:93623600-93631200	Strong transcription	Primary B cells from peripheral blood	blood
22	chr9:93623600-93642400	Weak transcription	Adipose Nuclei	Adipose
23	chr9:93623800-93626800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr9:93623800-93630400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr9:93623800-93631000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr9:93623800-93631400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr9:93624000-93630000	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr9:93624000-93631200	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr9:93624200-93630000	Strong transcription	Fetal Intestine Large	intestine
30	chr9:93625000-93636600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:93625000-93642200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr9:93625200-93628600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:93625200-93642400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:93625600-93628800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr9:93625600-93629400	Weak transcription	Gastric	stomach
36	chr9:93625600-93636400	Weak transcription	Lung	lung
37	chr9:93625800-93635800	Weak transcription	Esophagus	oesophagus
38	chr9:93626000-93626800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr9:93626000-93647800	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr9:93626200-93627600	Enhancers	Primary T cells from cord blood	blood
41	chr9:93626200-93629200	Weak transcription	Colonic Mucosa	Colon
42	chr9:93626400-93627400	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr9:93626400-93627600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr9:93626400-93627600	Strong transcription	Small Intestine	intestine
45	chr9:93626400-93627800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr9:93626600-93627000	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr9:93626600-93627400	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr9:93626600-93627400	Genic enhancers	Fetal Thymus	thymus
49	chr9:93626600-93627600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr9:93626600-93627600	Enhancers	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links