Variant report

Variant	rs10119836
Chromosome Location	chr9:92692398-92692399
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:92687750..92690637-chr9:92691262..92693318,3	MCF-7	breast:
2	chr9:92691934..92694632-chr9:92847404..92848934,2	MCF-7	breast:
3	chr9:92218809..92222310-chr9:92690732..92694174,4	MCF-7	breast:
4	chr9:92689850..92692779-chr9:92694377..92697288,2	MCF-7	breast:
5	chr9:92691647..92693844-chr9:92695816..92697738,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000130222	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10118987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10121885	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124931	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10991742	1.00[YRI][hapmap]
rs10991825	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12348128	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16905909	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28391004	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28451518	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28588897	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28615383	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2890108	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58357255	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59021050	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59052558	0.82[ASN][1000 genomes]
rs59127989	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60120851	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7018468	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73649353	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv15329	chr9:92678855-92698160	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92689000-92693000	Enhancers	Right Ventricle	heart
2	chr9:92689200-92692400	Enhancers	NHDF-Ad	bronchial
3	chr9:92689200-92693000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr9:92689200-92693200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr9:92689200-92693400	Enhancers	Fetal Muscle Leg	muscle
6	chr9:92689200-92694000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr9:92689600-92692400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:92689800-92697000	Weak transcription	Gastric	stomach
9	chr9:92689800-92697800	Weak transcription	Brain Angular Gyrus	brain
10	chr9:92690000-92692600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr9:92690000-92697400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr9:92690400-92692800	Enhancers	Left Ventricle	heart
13	chr9:92690400-92693200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:92690600-92692800	Enhancers	Psoas Muscle	Psoas
15	chr9:92690800-92695400	Weak transcription	Liver	Liver
16	chr9:92690800-92695600	Weak transcription	Ovary	ovary
17	chr9:92691000-92693000	Enhancers	Brain Germinal Matrix	brain
18	chr9:92691000-92693200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:92691000-92693400	Enhancers	Fetal Thymus	thymus
20	chr9:92691200-92693000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:92691200-92693000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr9:92691200-92693000	Enhancers	Spleen	Spleen
23	chr9:92691200-92693000	Enhancers	HSMM	muscle
24	chr9:92691200-92693000	Enhancers	HSMMtube	muscle
25	chr9:92691200-92693200	Enhancers	Fetal Heart	heart
26	chr9:92691200-92693200	Enhancers	Fetal Lung	lung
27	chr9:92691200-92693200	Enhancers	Dnd41	blood
28	chr9:92691200-92693400	Enhancers	Fetal Kidney	kidney
29	chr9:92691200-92693800	Enhancers	Primary T cells from cord blood	blood
30	chr9:92691200-92693800	Enhancers	Primary hematopoietic stem cells	blood
31	chr9:92691400-92692600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr9:92691400-92692800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:92691400-92692800	Enhancers	Fetal Intestine Small	intestine
34	chr9:92691400-92693000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:92691400-92693200	Enhancers	Fetal Stomach	stomach
36	chr9:92691400-92693600	Enhancers	Placenta	Placenta
37	chr9:92691400-92693800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:92691600-92692600	Weak transcription	Lung	lung
39	chr9:92691600-92692800	Enhancers	Fetal Intestine Large	intestine
40	chr9:92691600-92692800	Enhancers	HUVEC	blood vessel
41	chr9:92691600-92693000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:92691600-92693000	Enhancers	NH-A	brain
43	chr9:92691600-92693000	Enhancers	NHLF	lung
44	chr9:92691600-92693400	Enhancers	Adipose Nuclei	Adipose
45	chr9:92691600-92693400	Enhancers	Fetal Muscle Trunk	muscle
46	chr9:92691600-92693400	Enhancers	Right Atrium	heart
47	chr9:92691600-92694000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr9:92691800-92692800	Enhancers	Osteobl	bone
49	chr9:92692000-92692400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr9:92692000-92692600	Enhancers	Sigmoid Colon	Sigmoid Colon

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