Variant report

Variant	rs1333632
Chromosome Location	chr9:93567732-93567733
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:93561656..93565893-chr9:93566155..93575937,12	MCF-7	breast:
2	chr9:93566479..93568925-chr9:93571004..93572513,2	MCF-7	breast:
3	chr9:93566130..93568297-chr9:93575356..93577751,2	K562	blood:
4	chr9:93566333..93568000-chr9:93577767..93579301,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165025	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1319677	0.86[ASN][1000 genomes]
rs1333633	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1333634	0.89[ASN][1000 genomes]
rs1333635	0.85[ASN][1000 genomes]
rs2562396	0.89[ASN][1000 genomes]
rs2562397	0.81[ASN][1000 genomes]
rs2613308	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2774260	0.89[ASN][1000 genomes]
rs2780701	0.89[ASN][1000 genomes]
rs2780702	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs290987	0.82[ASN][1000 genomes]
rs290988	0.82[ASN][1000 genomes]
rs290989	0.82[ASN][1000 genomes]
rs290990	0.82[ASN][1000 genomes]
rs290991	0.80[ASN][1000 genomes]
rs290992	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs290993	0.82[ASN][1000 genomes]
rs290994	0.82[ASN][1000 genomes]
rs290997	0.82[ASN][1000 genomes]
rs7036417	0.87[ASN][1000 genomes]
rs7041684	0.87[ASN][1000 genomes]
rs772407	0.82[ASN][1000 genomes]
rs919386	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv893567	chr9:93519280-93609668	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	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
4	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
5	nsv893569	chr9:93552550-93587089	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	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
7	esv1813758	chr9:93557698-93573095	Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv275555	chr9:93565999-93570451	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1333632	SYK	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93563200-93568000	Flanking Active TSS	Primary hematopoietic stem cells	blood
2	chr9:93564600-93568600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:93564600-93572000	Weak transcription	Lung	lung
4	chr9:93564800-93567800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:93565000-93569400	Weak transcription	Primary T cells from cord blood	blood
6	chr9:93565000-93609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:93565200-93567800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr9:93565200-93568400	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr9:93565400-93570600	Weak transcription	HMEC	breast
10	chr9:93565400-93570800	Weak transcription	Placenta	Placenta
11	chr9:93565400-93577000	Weak transcription	Colonic Mucosa	Colon
12	chr9:93565600-93567800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr9:93566200-93567800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr9:93566200-93567800	Enhancers	Fetal Lung	lung
15	chr9:93566800-93567800	Enhancers	K562	blood
16	chr9:93566800-93568400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr9:93566800-93569200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr9:93567000-93567800	Enhancers	Fetal Intestine Large	intestine
19	chr9:93567000-93572800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr9:93567200-93568000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:93567200-93568600	Flanking Active TSS	GM12878-XiMat	blood
22	chr9:93567400-93567800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr9:93567400-93567800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr9:93567400-93567800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr9:93567400-93567800	Enhancers	Brain Germinal Matrix	brain
26	chr9:93567400-93567800	Flanking Active TSS	Duodenum Mucosa	Duodenum
27	chr9:93567400-93567800	Enhancers	Esophagus	oesophagus
28	chr9:93567400-93567800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr9:93567400-93567800	Enhancers	Gastric	stomach
30	chr9:93567400-93567800	Enhancers	Pancreas	Pancrea
31	chr9:93567400-93567800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr9:93567400-93567800	Enhancers	Small Intestine	intestine
33	chr9:93567400-93567800	Enhancers	Stomach Mucosa	stomach
34	chr9:93567400-93567800	Flanking Active TSS	Thymus	Thymus
35	chr9:93567400-93567800	Enhancers	Spleen	Spleen
36	chr9:93567400-93568000	Flanking Active TSS	Primary B cells from peripheral blood	blood
37	chr9:93567400-93570000	Enhancers	Fetal Stomach	stomach
38	chr9:93567600-93567800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr9:93567600-93567800	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr9:93567600-93567800	Flanking Active TSS	Fetal Thymus	thymus
41	chr9:93567600-93567800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
42	chr9:93567600-93567800	Bivalent Enhancer	Dnd41	blood
43	chr9:93567600-93568000	Enhancers	Fetal Kidney	kidney
44	chr9:93567600-93571000	Weak transcription	Fetal Intestine Small	intestine
45	chr9:93567600-93573000	Weak transcription	NHEK	skin

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