Variant report

Variant	rs9833428
Chromosome Location	chr3:24640958-24640959
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:24639170..24642285-chr3:24644377..24647650,4	K562	blood:
2	chr3:24534578..24538584-chr3:24640482..24644285,4	K562	blood:
3	chr3:24633657..24635628-chr3:24639189..24641484,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151090	Chromatin interaction
ENSG00000228791	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17014897	1.00[EUR][1000 genomes]
rs55783210	1.00[EUR][1000 genomes]
rs56835827	1.00[EUR][1000 genomes]
rs73820006	1.00[EUR][1000 genomes]
rs73820011	1.00[EUR][1000 genomes]
rs73826118	1.00[EUR][1000 genomes]
rs73826119	1.00[EUR][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	nsv999384	chr3:24525345-24656873	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24635600-24641400	Enhancers	HMEC	breast
2	chr3:24637000-24641000	Enhancers	NHEK	skin
3	chr3:24639400-24641400	Enhancers	Hela-S3	cervix
4	chr3:24639800-24641200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:24639800-24641400	Enhancers	Stomach Mucosa	stomach
6	chr3:24639800-24642000	Enhancers	Fetal Intestine Large	intestine
7	chr3:24639800-24642000	Enhancers	Fetal Intestine Small	intestine
8	chr3:24640000-24641000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr3:24640000-24641200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:24640000-24641200	Enhancers	Duodenum Mucosa	Duodenum
11	chr3:24640000-24641200	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr3:24640000-24642600	Enhancers	Fetal Lung	lung
13	chr3:24640200-24644200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:24640400-24641000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:24640400-24641000	Enhancers	HUVEC	blood vessel
16	chr3:24640400-24643600	Weak transcription	NHDF-Ad	bronchial
17	chr3:24640400-24645400	Weak transcription	HepG2	liver
18	chr3:24640600-24641000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr3:24640600-24641000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:24640600-24641000	Enhancers	Adipose Nuclei	Adipose
21	chr3:24640800-24641000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:24640800-24641000	Enhancers	Liver	Liver
23	chr3:24640800-24641000	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr3:24640800-24641000	Enhancers	Small Intestine	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links