Variant report

Variant	rs7448528
Chromosome Location	chr5:117885899-117885900
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10035809	0.84[EUR][1000 genomes]
rs10038758	0.84[EUR][1000 genomes]
rs10050514	0.91[EUR][1000 genomes]
rs10050645	0.92[EUR][1000 genomes]
rs10051807	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10052243	0.92[EUR][1000 genomes]
rs10054774	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10058452	0.90[EUR][1000 genomes]
rs10058652	0.92[EUR][1000 genomes]
rs10058989	0.94[EUR][1000 genomes]
rs10068932	0.94[EUR][1000 genomes]
rs10069611	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10519555	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12110271	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13187515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1429728	0.94[ASN][1000 genomes]
rs1429730	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1429731	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1864330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1864331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34196702	0.85[EUR][1000 genomes]
rs34450294	0.94[EUR][1000 genomes]
rs34457532	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35034186	0.93[EUR][1000 genomes]
rs35558754	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35561449	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35767330	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs36020800	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs36072947	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62370364	0.92[EUR][1000 genomes]
rs62370365	0.93[EUR][1000 genomes]
rs62370384	0.82[EUR][1000 genomes]
rs66500274	0.88[EUR][1000 genomes]
rs66524140	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6885538	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6885552	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6885715	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72795552	0.87[EUR][1000 genomes]
rs72795554	0.88[EUR][1000 genomes]
rs72795555	0.91[EUR][1000 genomes]
rs7704356	0.89[EUR][1000 genomes]
rs7705821	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7716116	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7718877	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7719858	0.84[EUR][1000 genomes]
rs7737007	0.88[EUR][1000 genomes]
rs7737327	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7737856	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs970368	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027428	chr5:117072745-118036353	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv537877	chr5:117072745-118036353	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv1067621	chr5:117102544-118036352	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv531292	chr5:117102544-118036352	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	esv2422395	chr5:117442806-117887910	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv432802	chr5:117612408-117921244	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	esv2758013	chr5:117664725-117942247	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
8	esv2759373	chr5:117664725-117942247	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv462422	chr5:117740545-118020706	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	nsv599529	chr5:117740545-118020706	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
11	nsv427731	chr5:117781143-118023504	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
12	nsv1021863	chr5:117832733-117955524	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv462424	chr5:117843869-117955570	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv599539	chr5:117843869-117955570	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv462425	chr5:117843869-117967472	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv599540	chr5:117843869-117967472	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
17	nsv599541	chr5:117869174-118049776	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
18	nsv1024374	chr5:117882620-117909965	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv882764	chr5:117884766-118014946	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117883600-117887200	Enhancers	HMEC	breast
2	chr5:117883600-117887400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:117883600-117890800	Enhancers	NHDF-Ad	bronchial
4	chr5:117883800-117891400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:117884200-117886000	Enhancers	NHLF	lung
6	chr5:117884200-117887200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:117885000-117892600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:117885200-117886000	Weak transcription	Brain Germinal Matrix	brain
9	chr5:117885200-117889200	Weak transcription	Osteobl	bone
10	chr5:117885200-117890800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:117885200-117894200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:117885400-117886800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:117885400-117889200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr5:117885400-117889600	Weak transcription	NH-A	brain
15	chr5:117885600-117887000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:117885800-117886200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:117885800-117892600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links