Variant report

Variant	rs17277467
Chromosome Location	chr9:13939884-13939885
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10810058	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10961339	0.86[JPT][hapmap]
rs13283645	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13283743	0.86[JPT][hapmap]
rs13285663	0.93[ASN][1000 genomes]
rs13286204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13291088	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13292270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13292571	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13298062	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13299074	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13299961	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17192194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17277593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17278798	0.88[JPT][hapmap]
rs34602246	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs34660040	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs34764349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35165583	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35246532	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35249758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35377705	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35684545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35727886	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35907479	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35911657	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35960404	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs55776100	0.81[ASN][1000 genomes]
rs7023574	0.86[JPT][hapmap]
rs71511071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71511072	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022001	chr9:13717736-13983738	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1033764	chr9:13764918-14226168	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv613635	chr9:13893246-13961462	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1015319	chr9:13931836-13970419	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv613636	chr9:13936438-13975480	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13933600-13961600	Weak transcription	Psoas Muscle	Psoas
2	chr9:13936200-13942000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr9:13937400-13940000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr9:13938000-13940000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:13938000-13940600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:13938000-13943000	Enhancers	Fetal Lung	lung
7	chr9:13938200-13940800	Enhancers	HMEC	breast
8	chr9:13938200-13941000	Enhancers	Fetal Heart	heart
9	chr9:13938400-13940800	Enhancers	Osteobl	bone
10	chr9:13938400-13948000	Weak transcription	Right Ventricle	heart
11	chr9:13938600-13940000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:13938600-13940000	Enhancers	Hela-S3	cervix
13	chr9:13938600-13940000	Enhancers	NHDF-Ad	bronchial
14	chr9:13938600-13940200	Enhancers	HUVEC	blood vessel
15	chr9:13938600-13942000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr9:13938800-13940000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr9:13938800-13940000	Enhancers	Aorta	Aorta
18	chr9:13938800-13940200	Enhancers	Ovary	ovary
19	chr9:13938800-13940600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:13938800-13940600	Enhancers	HSMM	muscle
21	chr9:13939000-13940000	Enhancers	NH-A	brain
22	chr9:13939000-13940800	Enhancers	Fetal Muscle Leg	muscle
23	chr9:13939400-13940000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr9:13939400-13940000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:13939400-13940000	Enhancers	Pancreas	Pancrea
26	chr9:13939400-13940000	Enhancers	NHLF	lung
27	chr9:13939400-13940200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:13939400-13940400	Enhancers	HSMMtube	muscle
29	chr9:13939400-13940600	Enhancers	Stomach Mucosa	stomach
30	chr9:13939600-13940000	Enhancers	Adipose Nuclei	Adipose
31	chr9:13939600-13940000	Enhancers	Brain Hippocampus Middle	brain
32	chr9:13939600-13940000	Enhancers	Duodenum Mucosa	Duodenum
33	chr9:13939600-13940000	Enhancers	Fetal Muscle Trunk	muscle
34	chr9:13939600-13940000	Enhancers	Right Atrium	heart
35	chr9:13939600-13940000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr9:13939600-13940400	Enhancers	Left Ventricle	heart
37	chr9:13939600-13940600	Enhancers	Brain Germinal Matrix	brain
38	chr9:13939600-13944000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:13939600-13944200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:13939800-13941800	Weak transcription	Fetal Stomach	stomach
41	chr9:13939800-13942200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:13939800-13942200	Weak transcription	NHEK	skin
43	chr9:13939800-13956200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links