Variant report

Variant	rs1445989
Chromosome Location	chr5:52460580-52460581
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	chr5:52454172..52456744-chr5:52460195..52462094,2	MCF-7	breast:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1445990	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1808399	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs251587	0.81[AMR][1000 genomes]
rs254473	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs254487	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs254488	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2591904	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs30637	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs30714	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs964937	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs964938	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52458200-52461800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr5:52458200-52463600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr5:52458200-52463600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr5:52458200-52463600	Weak transcription	Osteobl	bone
5	chr5:52458400-52461400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:52458800-52461800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr5:52459600-52461200	Enhancers	Liver	Liver
8	chr5:52460000-52460800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:52460000-52465200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:52460200-52461200	Enhancers	HepG2	liver
11	chr5:52460200-52462600	Enhancers	Fetal Lung	lung
12	chr5:52460200-52462800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr5:52460200-52464400	Enhancers	NHDF-Ad	bronchial
14	chr5:52460400-52460600	Enhancers	Fetal Brain Male	brain
15	chr5:52460400-52460800	Enhancers	Left Ventricle	heart
16	chr5:52460400-52460800	Enhancers	Right Atrium	heart
17	chr5:52460400-52460800	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr5:52460400-52460800	Enhancers	Stomach Smooth Muscle	stomach
19	chr5:52460400-52461000	Enhancers	Fetal Muscle Leg	muscle
20	chr5:52460400-52462800	Enhancers	Fetal Stomach	stomach
21	chr5:52460400-52464200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:52460400-52465200	Enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links