Variant report

Variant	rs12551506
Chromosome Location	chr9:97703028-97703029
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:97702356..97704660-chr9:97713620..97715867,3	MCF-7	breast:
2	chr9:97701079..97703589-chr9:97706608..97709987,3	K562	blood:
3	chr9:97702032..97704710-chr9:97710037..97711547,2	K562	blood:

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs1004813	0.82[JPT][hapmap]
rs10125566	0.84[AMR][1000 genomes]
rs10217441	0.84[AMR][1000 genomes]
rs10512252	0.82[JPT][hapmap]
rs10732407	0.84[AMR][1000 genomes]
rs10739988	0.84[AMR][1000 genomes]
rs10739990	0.84[AMR][1000 genomes]
rs10739991	0.82[JPT][hapmap]
rs10761362	0.81[AMR][1000 genomes]
rs10821411	0.84[AMR][1000 genomes]
rs10993435	1.00[CEU][hapmap]
rs10993449	1.00[CEU][hapmap]
rs1113967	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs12552838	1.00[AMR][1000 genomes]
rs12554043	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12682668	0.82[JPT][hapmap]
rs12683896	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12684139	0.82[JPT][hapmap]
rs12684154	0.82[JPT][hapmap]
rs12684461	0.82[JPT][hapmap]
rs12684470	0.82[JPT][hapmap]
rs12686277	0.82[JPT][hapmap]
rs12686500	0.82[JPT][hapmap]
rs1382411	0.88[AMR][1000 genomes]
rs1382412	0.88[AMR][1000 genomes]
rs1530331	0.82[JPT][hapmap]
rs1542107	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs1571897	1.00[JPT][hapmap]
rs16905557	0.82[JPT][hapmap]
rs16911801	0.82[JPT][hapmap]
rs16911802	0.82[JPT][hapmap]
rs16911817	0.82[JPT][hapmap]
rs16911821	0.82[JPT][hapmap]
rs16911826	0.82[JPT][hapmap]
rs16911834	1.00[AMR][1000 genomes]
rs16911856	0.80[AMR][1000 genomes]
rs1806996	0.82[JPT][hapmap]
rs1904201	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2026399	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2078379	0.82[JPT][hapmap]
rs2095069	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2119953	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs2406897	0.84[AMR][1000 genomes]
rs2406898	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs2896816	1.00[CEU][hapmap]
rs2897523	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs3824493	0.82[JPT][hapmap]
rs3847309	0.82[JPT][hapmap]
rs3847310	0.82[JPT][hapmap]
rs3847311	0.81[AMR][1000 genomes]
rs3886567	0.82[JPT][hapmap]
rs3886568	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs41316526	0.88[AMR][1000 genomes]
rs4332191	0.84[AMR][1000 genomes]
rs4743976	0.85[JPT][hapmap]
rs4744389	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs6479568	0.82[JPT][hapmap]
rs6479576	0.82[JPT][hapmap]
rs6479581	0.84[AMR][1000 genomes]
rs66642068	0.88[AMR][1000 genomes]
rs66863985	0.88[AMR][1000 genomes]
rs66993340	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67490803	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67756624	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7019602	0.84[AMR][1000 genomes]
rs7026714	0.82[JPT][hapmap]
rs7029570	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7035166	0.82[JPT][hapmap]
rs7038519	0.82[JPT][hapmap]
rs7042271	1.00[CEU][hapmap]
rs7044371	0.84[AMR][1000 genomes]
rs7045005	0.82[JPT][hapmap]
rs7046900	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72748601	1.00[AMR][1000 genomes]
rs73538177	0.88[AMR][1000 genomes]
rs7465900	0.82[JPT][hapmap]
rs7850601	0.82[JPT][hapmap]
rs7850680	0.82[JPT][hapmap]
rs7869736	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs7870679	0.82[JPT][hapmap]
rs894426	0.84[AMR][1000 genomes]
rs894427	0.82[JPT][hapmap];0.84[AMR][1000 genomes]
rs894428	0.82[JPT][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	nsv933919	chr9:97619512-97919344	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
2	nsv1045849	chr9:97688810-97741336	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97670600-97766000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr9:97682000-97713800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr9:97684800-97711000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:97685200-97714600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr9:97687000-97714000	Weak transcription	Thymus	Thymus
6	chr9:97691400-97703400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:97691800-97710800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr9:97692200-97713000	Weak transcription	Primary T cells from cord blood	blood
9	chr9:97692400-97707600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr9:97693400-97712600	Weak transcription	Gastric	stomach
11	chr9:97695600-97709000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:97699200-97703200	Weak transcription	Fetal Kidney	kidney
13	chr9:97699600-97703600	Weak transcription	Fetal Lung	lung
14	chr9:97699800-97706400	Weak transcription	Brain Angular Gyrus	brain
15	chr9:97700000-97703400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr9:97700200-97703400	Weak transcription	Brain Cingulate Gyrus	brain
17	chr9:97700200-97703600	Weak transcription	HMEC	breast
18	chr9:97700200-97707200	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:97700200-97707400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:97700200-97707400	Weak transcription	Brain Substantia Nigra	brain
21	chr9:97700200-97707600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr9:97700200-97707600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr9:97700200-97707800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:97700200-97708200	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:97700200-97714600	Weak transcription	Fetal Stomach	stomach
26	chr9:97700200-97718600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:97700400-97707200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr9:97700600-97703200	Weak transcription	Fetal Heart	heart
29	chr9:97700600-97703400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:97700600-97706600	Weak transcription	NHEK	skin
31	chr9:97700800-97703200	Weak transcription	NH-A	brain
32	chr9:97700800-97703400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:97701000-97703200	Weak transcription	NHLF	lung
34	chr9:97701000-97703400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:97701200-97707600	Weak transcription	K562	blood
36	chr9:97702200-97703400	Enhancers	HepG2	liver
37	chr9:97702400-97703200	Enhancers	A549	lung
38	chr9:97702400-97704000	Enhancers	Stomach Mucosa	stomach
39	chr9:97702400-97704600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr9:97702400-97705000	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr9:97702600-97703400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr9:97702600-97704000	Genic enhancers	Fetal Muscle Leg	muscle
43	chr9:97702600-97704000	Enhancers	Lung	lung
44	chr9:97702600-97704000	Enhancers	Psoas Muscle	Psoas
45	chr9:97702600-97704000	Enhancers	Right Atrium	heart
46	chr9:97702600-97704800	Enhancers	Fetal Intestine Small	intestine
47	chr9:97702600-97705200	Enhancers	Fetal Intestine Large	intestine
48	chr9:97702800-97704000	Enhancers	Small Intestine	intestine
49	chr9:97703000-97703600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:97703000-97703600	Enhancers	Placenta	Placenta

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