Variant report

Variant	rs7037618
Chromosome Location	chr9:13182414-13182415
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10116304	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10116749	0.85[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10120857	0.92[ASN][1000 genomes]
rs10122431	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10125770	0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs10511577	0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10733254	0.86[ASN][1000 genomes]
rs10738323	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs10738324	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10738325	0.86[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs10756454	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10756455	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs10756456	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10756457	0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs10756458	0.88[ASN][1000 genomes]
rs10756459	0.86[ASN][1000 genomes]
rs10756460	0.98[ASN][1000 genomes]
rs10809906	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10809907	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10809912	0.87[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10809913	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10809920	0.86[JPT][hapmap]
rs10960955	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10960958	0.87[ASN][1000 genomes]
rs10960959	0.83[ASN][1000 genomes]
rs12351444	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1330129	0.95[JPT][hapmap]
rs1331668	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs1331670	0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs1331672	0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1331673	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1331674	0.90[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1331675	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1360058	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1556421	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs16930137	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1854907	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1854908	1.00[JPT][hapmap]
rs1854909	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1929541	0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1999393	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2225483	0.82[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs2274856	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2297003	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs3818595	0.95[JPT][hapmap]
rs4237130	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs4741291	0.87[CHB][hapmap]
rs58794982	0.80[ASN][1000 genomes]
rs6474753	0.87[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6474754	0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6474755	0.85[ASN][1000 genomes]
rs7024892	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs7035244	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7037704	0.85[ASN][1000 genomes]
rs7040347	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs72706366	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7859465	0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7867993	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs7871575	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs9886797	0.82[CHB][hapmap];0.95[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	nsv892578	chr9:12942956-13485035	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv892583	chr9:13166139-13350478	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13121600-13225200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr9:13122600-13186400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:13135400-13223600	Weak transcription	Lung	lung
4	chr9:13136000-13192400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:13138800-13191800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr9:13139000-13188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:13141000-13197800	Weak transcription	NHDF-Ad	bronchial
8	chr9:13141200-13188200	Weak transcription	NHLF	lung
9	chr9:13143600-13202200	Weak transcription	Pancreas	Pancrea
10	chr9:13145400-13203200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:13145400-13228600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr9:13146600-13202400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr9:13150000-13193200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr9:13153200-13194800	Weak transcription	Fetal Kidney	kidney
15	chr9:13156800-13201400	Weak transcription	Psoas Muscle	Psoas
16	chr9:13158800-13188800	Weak transcription	Fetal Heart	heart
17	chr9:13160600-13183000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr9:13161600-13188200	Weak transcription	Fetal Stomach	stomach
19	chr9:13162200-13188200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:13163600-13202000	Weak transcription	Rectal Smooth Muscle	rectum
21	chr9:13164200-13188000	Weak transcription	Brain Hippocampus Middle	brain
22	chr9:13164200-13188800	Weak transcription	Brain Substantia Nigra	brain
23	chr9:13164200-13248600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr9:13164200-13258800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:13165800-13187400	Weak transcription	Brain Germinal Matrix	brain
26	chr9:13168000-13201800	Weak transcription	Colon Smooth Muscle	Colon
27	chr9:13168400-13182600	Weak transcription	Fetal Lung	lung
28	chr9:13168400-13188200	Weak transcription	Brain Cingulate Gyrus	brain
29	chr9:13168600-13188200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr9:13170000-13188200	Weak transcription	Left Ventricle	heart
31	chr9:13173000-13188800	Weak transcription	Spleen	Spleen
32	chr9:13175200-13188200	Weak transcription	Aorta	Aorta
33	chr9:13175800-13203000	Weak transcription	Fetal Intestine Small	intestine
34	chr9:13176200-13187800	Weak transcription	Placenta	Placenta
35	chr9:13176400-13182600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr9:13176400-13183200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr9:13176400-13186800	Weak transcription	Ovary	ovary
38	chr9:13176400-13187000	Weak transcription	Fetal Muscle Trunk	muscle
39	chr9:13176400-13187600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr9:13176400-13187800	Weak transcription	Osteobl	bone
41	chr9:13176400-13188200	Weak transcription	Fetal Muscle Leg	muscle
42	chr9:13176400-13188800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:13176400-13202600	Weak transcription	Duodenum Mucosa	Duodenum
44	chr9:13176600-13184000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr9:13176600-13191800	Weak transcription	Fetal Intestine Large	intestine
46	chr9:13177600-13197400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:13179800-13183800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:13179800-13183800	Strong transcription	Adipose Nuclei	Adipose
49	chr9:13179800-13184000	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr9:13179800-13196600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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