Variant report

Variant	rs17146635
Chromosome Location	chr5:119789295-119789296
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:119784118..119786225-chr5:119788090..119789969,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12109029	0.89[ASN][1000 genomes]
rs13359009	1.00[ASN][1000 genomes]
rs1432461	1.00[ASN][1000 genomes]
rs1432462	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1503926	0.82[YRI][hapmap];0.80[AFR][1000 genomes]
rs1503928	0.84[EUR][1000 genomes]
rs1503929	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17146602	0.80[EUR][1000 genomes]
rs17146628	0.82[AMR][1000 genomes]
rs17146632	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17146644	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17424128	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17489517	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17489671	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17489720	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4895253	0.83[ASN][1000 genomes]
rs56398366	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57401201	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58699148	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58831848	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60249515	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61113370	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66523245	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72784190	0.80[EUR][1000 genomes]
rs72784191	0.81[EUR][1000 genomes]
rs72784195	0.80[EUR][1000 genomes]
rs72784197	0.82[EUR][1000 genomes]
rs72784200	0.80[EUR][1000 genomes]
rs72784202	0.85[EUR][1000 genomes]
rs72786208	0.82[EUR][1000 genomes]
rs72786223	0.82[EUR][1000 genomes]
rs72786224	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72786225	0.84[EUR][1000 genomes]
rs72786226	0.84[EUR][1000 genomes]
rs72786229	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73783447	0.80[AFR][1000 genomes]
rs73785931	0.82[AFR][1000 genomes]
rs7730105	0.84[EUR][1000 genomes]
rs7734475	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9327142	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1018955	chr5:119679918-119802014	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1018100	chr5:119749898-119802014	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119782800-119790000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:119783000-119793600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr5:119783800-119790000	Weak transcription	NHLF	lung
4	chr5:119785600-119789400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:119785600-119789800	Weak transcription	Osteobl	bone
6	chr5:119785800-119789600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:119785800-119789800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:119786200-119793600	Weak transcription	Right Ventricle	heart
9	chr5:119786200-119793800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:119786800-119789400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr5:119787000-119798200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:119787400-119790800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:119787400-119793000	Weak transcription	Pancreas	Pancrea
14	chr5:119787400-119799600	Weak transcription	Psoas Muscle	Psoas
15	chr5:119787600-119790000	Enhancers	HSMMtube	muscle
16	chr5:119787600-119791000	Enhancers	HSMM	muscle
17	chr5:119788000-119790000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr5:119788600-119790000	Weak transcription	NH-A	brain
19	chr5:119788800-119790600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr5:119788800-119794000	Enhancers	Fetal Heart	heart
21	chr5:119789200-119790000	Enhancers	NHDF-Ad	bronchial
22	chr5:119789200-119790200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:119789200-119791000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr5:119789200-119791200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:119789200-119791200	Enhancers	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links