Variant report

Variant	rs9548830
Chromosome Location	chr13:40146469-40146470
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1885759	1.00[CEU][hapmap]
rs2324337	0.96[CEU][hapmap]
rs7318072	0.84[GIH][hapmap];0.91[MEX][hapmap]
rs7322336	1.00[CEU][hapmap]
rs7333056	1.00[CEU][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap]
rs7982917	0.92[CEU][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap]
rs9315701	0.96[CEU][hapmap]
rs9315702	0.96[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs9315703	0.92[CEU][hapmap];0.80[MEX][hapmap];0.81[TSI][hapmap]
rs9315706	1.00[CEU][hapmap]
rs9315707	0.88[ASW][hapmap];1.00[CEU][hapmap];0.81[LWK][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap]
rs9548805	0.92[CEU][hapmap]
rs9548809	0.91[CEU][hapmap]
rs9548819	0.92[CEU][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap]
rs9548825	1.00[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs9548826	1.00[CEU][hapmap]
rs9548829	1.00[CEU][hapmap]
rs9576852	0.81[JPT][hapmap];0.80[YRI][hapmap]

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	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9548830	FOXO1	cis	parietal	SCAN

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40129000-40152800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:40138800-40152800	Weak transcription	Aorta	Aorta
3	chr13:40139200-40158000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:40140000-40169400	Weak transcription	Fetal Stomach	stomach
5	chr13:40140200-40149600	Weak transcription	Fetal Muscle Leg	muscle
6	chr13:40140400-40157800	Weak transcription	Adipose Nuclei	Adipose
7	chr13:40140600-40146600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:40140600-40148600	Weak transcription	Fetal Lung	lung
9	chr13:40140800-40152800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr13:40140800-40165400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr13:40142000-40148800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr13:40142000-40156200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:40142000-40156200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr13:40142000-40169400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr13:40142000-40169400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:40142200-40150000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:40142200-40152600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr13:40143000-40149400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr13:40143000-40158200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr13:40143200-40157800	Weak transcription	NHDF-Ad	bronchial
21	chr13:40143200-40161800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr13:40143200-40170800	Weak transcription	Osteobl	bone
23	chr13:40144400-40147200	Enhancers	Fetal Heart	heart
24	chr13:40145600-40146800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:40145600-40153200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:40146000-40146800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr13:40146000-40149800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr13:40146000-40152800	Weak transcription	NHLF	lung
29	chr13:40146000-40155400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr13:40146000-40171800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr13:40146200-40146800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:40146200-40149000	Weak transcription	Fetal Muscle Trunk	muscle
33	chr13:40146200-40149800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:40146200-40151000	Weak transcription	Ovary	ovary
35	chr13:40146200-40151800	Weak transcription	Lung	lung
36	chr13:40146200-40161400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr13:40146400-40146600	Enhancers	Brain Substantia Nigra	brain
38	chr13:40146400-40146800	Weak transcription	Left Ventricle	heart
39	chr13:40146400-40146800	Weak transcription	Right Atrium	heart
40	chr13:40146400-40146800	Weak transcription	Right Ventricle	heart
41	chr13:40146400-40149800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr13:40146400-40155200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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