Variant report

Variant	rs1093703
Chromosome Location	chr9:7024194-7024195
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10815511	0.82[JPT][hapmap]
rs1093705	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10975974	0.99[ASN][1000 genomes]
rs10975989	0.85[EUR][1000 genomes]
rs10975997	0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs1175020	0.94[AMR][1000 genomes]
rs1544055	0.82[JPT][hapmap]
rs1570509	0.82[JPT][hapmap]
rs1570513	0.82[JPT][hapmap]
rs2031199	0.80[JPT][hapmap]
rs2381540	0.82[JPT][hapmap]
rs2381541	0.88[JPT][hapmap]
rs2381542	0.88[JPT][hapmap]
rs2381544	0.83[JPT][hapmap]
rs3898792	0.82[JPT][hapmap]
rs4742298	0.82[JPT][hapmap]
rs57814978	0.89[ASN][1000 genomes]
rs6477143	0.83[JPT][hapmap]
rs6477150	0.82[JPT][hapmap]
rs7031179	0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs73639491	0.81[ASN][1000 genomes]
rs7851112	0.88[AMR][1000 genomes]
rs7852014	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs864696	0.91[ASN][1000 genomes]
rs866566	0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892166	chr9:6602821-7222495	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv892181	chr9:6680477-7070962	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
3	nsv1023906	chr9:6731786-7372132	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv831501	chr9:6868099-7058526	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv892185	chr9:6929053-7070962	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv870178	chr9:6941584-7060029	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv892186	chr9:6942605-7075305	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv892187	chr9:6974101-7035727	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv949711	chr9:6994399-7045058	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv892188	chr9:6999846-7026860	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv613257	chr9:7015330-7037370	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1024763	chr9:7022554-7061314	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1093703	JMJD2C	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6985600-7035600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:7008800-7024200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:7009000-7026200	Weak transcription	A549	lung
4	chr9:7009000-7027400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr9:7009000-7027800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:7009000-7027800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr9:7009000-7028400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:7009000-7030400	Weak transcription	NHEK	skin
9	chr9:7009000-7044800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:7009000-7046200	Weak transcription	Small Intestine	intestine
11	chr9:7009000-7055200	Weak transcription	K562	blood
12	chr9:7009000-7056400	Weak transcription	Brain Substantia Nigra	brain
13	chr9:7009000-7076600	Weak transcription	HSMM	muscle
14	chr9:7009200-7077600	Weak transcription	Osteobl	bone
15	chr9:7009400-7029600	Weak transcription	Hela-S3	cervix
16	chr9:7009400-7042000	Weak transcription	NHDF-Ad	bronchial
17	chr9:7009800-7076600	Weak transcription	HSMMtube	muscle
18	chr9:7011800-7048800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr9:7012200-7027400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr9:7012200-7027400	Weak transcription	Brain Anterior Caudate	brain
21	chr9:7012200-7027400	Weak transcription	Right Ventricle	heart
22	chr9:7012200-7027400	Weak transcription	Spleen	Spleen
23	chr9:7012200-7027600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:7012200-7046800	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr9:7012200-7052600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr9:7012200-7111200	Weak transcription	Colonic Mucosa	Colon
27	chr9:7012400-7028000	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr9:7012800-7027600	Weak transcription	Esophagus	oesophagus
29	chr9:7012800-7028400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr9:7012800-7048800	Weak transcription	Dnd41	blood
31	chr9:7012800-7076800	Weak transcription	Pancreas	Pancrea
32	chr9:7013800-7031800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr9:7014200-7027400	Weak transcription	Ovary	ovary
34	chr9:7014600-7048000	Weak transcription	Colon Smooth Muscle	Colon
35	chr9:7016000-7025200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:7016000-7036400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr9:7016200-7033200	Weak transcription	Rectal Smooth Muscle	rectum
38	chr9:7016800-7027600	Weak transcription	Fetal Stomach	stomach
39	chr9:7017000-7027200	Weak transcription	Aorta	Aorta
40	chr9:7017000-7027600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr9:7017200-7026000	Weak transcription	Fetal Intestine Small	intestine
42	chr9:7017200-7026600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr9:7017200-7027200	Weak transcription	Gastric	stomach
44	chr9:7017200-7028200	Weak transcription	Left Ventricle	heart
45	chr9:7017200-7028400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr9:7017200-7028800	Weak transcription	Fetal Muscle Leg	muscle
47	chr9:7017400-7027400	Weak transcription	Fetal Muscle Trunk	muscle
48	chr9:7017800-7027600	Weak transcription	Thymus	Thymus
49	chr9:7017800-7075000	Weak transcription	HepG2	liver
50	chr9:7018000-7027400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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