Variant report

Variant	rs7869264
Chromosome Location	chr9:116802539-116802540
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10116543	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10118282	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10982036	0.89[CEU][hapmap];0.85[GIH][hapmap];0.87[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10982037	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10982039	0.87[EUR][1000 genomes]
rs10982044	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10982046	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12378906	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12380714	1.00[GIH][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12555049	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1359171	0.89[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1359172	0.89[CEU][hapmap];0.85[GIH][hapmap];0.87[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1408115	0.88[YRI][hapmap]
rs16911753	0.89[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1965753	0.83[YRI][hapmap]
rs41277651	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7846976	0.89[CEU][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7856141	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv2422396	chr9:116792944-117354862	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116766600-116811200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr9:116773600-116809200	Weak transcription	Fetal Heart	heart
3	chr9:116785200-116811200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr9:116785400-116810600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr9:116787000-116803000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:116787000-116812800	Weak transcription	Primary B cells from cord blood	blood
7	chr9:116789600-116808600	Weak transcription	HMEC	breast
8	chr9:116790600-116802600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr9:116790600-116802600	Strong transcription	Liver	Liver
10	chr9:116792200-116802800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr9:116792200-116810400	Weak transcription	Thymus	Thymus
12	chr9:116793000-116802600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:116793200-116811200	Weak transcription	Stomach Mucosa	stomach
14	chr9:116793200-116812200	Weak transcription	K562	blood
15	chr9:116793200-116813800	Weak transcription	NHEK	skin
16	chr9:116795200-116802600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr9:116795200-116821800	Weak transcription	Right Atrium	heart
18	chr9:116796000-116802600	Strong transcription	A549	lung
19	chr9:116796000-116802800	Strong transcription	Fetal Lung	lung
20	chr9:116796200-116815800	Weak transcription	Small Intestine	intestine
21	chr9:116796800-116802800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:116797800-116802600	Strong transcription	Fetal Muscle Trunk	muscle
23	chr9:116798000-116802600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr9:116798000-116802600	Strong transcription	Ovary	ovary
25	chr9:116798000-116802800	Strong transcription	Fetal Muscle Leg	muscle
26	chr9:116798400-116802600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:116798400-116802600	Strong transcription	Osteobl	bone
28	chr9:116799000-116811200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr9:116799200-116811200	Weak transcription	Colon Smooth Muscle	Colon
30	chr9:116799400-116810600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr9:116799400-116810800	Weak transcription	Colonic Mucosa	Colon
32	chr9:116799600-116810200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr9:116799800-116802800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:116799800-116805400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr9:116799800-116810000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr9:116799800-116810200	Weak transcription	HSMMtube	muscle
37	chr9:116799800-116810600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr9:116800000-116809200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr9:116800000-116810200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr9:116800000-116810200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:116800000-116810800	Weak transcription	Brain Angular Gyrus	brain
42	chr9:116800000-116811200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr9:116800000-116811200	Weak transcription	Brain Substantia Nigra	brain
44	chr9:116800000-116811200	Weak transcription	Right Ventricle	heart
45	chr9:116800400-116805600	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr9:116800400-116810800	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr9:116800600-116802600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr9:116800600-116809800	Weak transcription	NHLF	lung
49	chr9:116800800-116802600	Strong transcription	Primary hematopoietic stem cells	blood
50	chr9:116800800-116802800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links