Variant report

Variant	rs9548796
Chromosome Location	chr13:40094490-40094491
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1022808	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1022810	0.82[CEU][hapmap];0.83[AMR][1000 genomes]
rs1160321	0.84[TSI][hapmap]
rs1570414	0.93[CEU][hapmap]
rs1885758	1.00[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs1885760	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1885761	0.83[AMR][1000 genomes]
rs1885762	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1885763	0.82[CEU][hapmap];0.84[AMR][1000 genomes]
rs1885764	0.84[AMR][1000 genomes]
rs2875329	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3812881	0.81[CEU][hapmap];0.84[AMR][1000 genomes]
rs4325425	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4520717	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4941933	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4941935	0.92[EUR][1000 genomes]
rs4943674	0.93[EUR][1000 genomes]
rs6563719	0.82[CEU][hapmap];0.83[AMR][1000 genomes]
rs6563720	1.00[CEU][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6563721	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6563726	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs6563727	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs7139592	0.84[AMR][1000 genomes]
rs7324883	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs7331023	1.00[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs7333587	0.93[CEU][hapmap];0.81[EUR][1000 genomes]
rs7985507	0.84[EUR][1000 genomes]
rs7988729	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs7992290	0.92[YRI][hapmap]
rs912050	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs9285135	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9285136	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9315698	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9315704	1.00[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs9315705	1.00[CEU][hapmap]
rs9548807	0.94[EUR][1000 genomes]
rs9566448	0.87[CEU][hapmap];0.89[TSI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9566457	0.93[CEU][hapmap]
rs9576865	1.00[CEU][hapmap];0.95[GIH][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes]
rs978135	1.00[CEU][hapmap];0.93[EUR][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	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1049669	chr13:40081362-40095803	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
4	esv2761784	chr13:40086325-40100095	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv1050137	chr13:40090742-40118499	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40076400-40096000	Weak transcription	Lung	lung
2	chr13:40077600-40101400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:40081600-40096000	Weak transcription	Fetal Lung	lung
4	chr13:40081600-40096600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:40090600-40094600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:40090600-40100800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr13:40090600-40102400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr13:40090800-40094600	Weak transcription	Ovary	ovary
9	chr13:40090800-40095800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:40090800-40095800	Weak transcription	Brain Substantia Nigra	brain
11	chr13:40090800-40095800	Weak transcription	NHEK	skin
12	chr13:40090800-40096000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr13:40090800-40102400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:40091200-40095800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr13:40091600-40095800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:40092200-40094600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr13:40093800-40097200	Enhancers	Fetal Heart	heart
18	chr13:40093800-40100800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr13:40094000-40095000	Enhancers	Right Atrium	heart
20	chr13:40094000-40095400	Enhancers	Left Ventricle	heart
21	chr13:40094200-40094600	Enhancers	Aorta	Aorta
22	chr13:40094200-40094600	Enhancers	Psoas Muscle	Psoas
23	chr13:40094200-40096800	Enhancers	Right Ventricle	heart
24	chr13:40094400-40095000	Enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links