Variant report

Variant	rs7921052
Chromosome Location	chr10:28346335-28346336
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10218925	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10219010	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10219011	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10740781	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10826389	0.90[EUR][1000 genomes]
rs10826390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10826393	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006815	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12217744	0.91[EUR][1000 genomes]
rs12570424	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3802520	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7077881	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7078263	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7078301	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7905976	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7920857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7920864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7921181	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv831815	chr10:28235661-28407533	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1052182	chr10:28259142-28361830	Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1042524	chr10:28290149-28506812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv831816	chr10:28304698-28493635	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv894988	chr10:28337570-28410989	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
7	nsv525448	chr10:28337570-28563732	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv466855	chr10:28341783-28400835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
9	nsv550284	chr10:28341783-28400835	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28336200-28349400	Weak transcription	Gastric	stomach
2	chr10:28336800-28346600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr10:28337400-28347400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:28341200-28350000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:28341200-28377600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr10:28341400-28346400	Weak transcription	Spleen	Spleen
7	chr10:28341800-28348600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr10:28341800-28349000	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr10:28341800-28349800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr10:28342400-28348400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr10:28342600-28350000	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr10:28342800-28347000	Weak transcription	HMEC	breast
13	chr10:28343600-28346400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr10:28343600-28346600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr10:28343800-28346600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr10:28344000-28355600	Weak transcription	Adipose Nuclei	Adipose
17	chr10:28344200-28346400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:28344200-28348600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:28344200-28349000	Weak transcription	Colon Smooth Muscle	Colon
20	chr10:28344400-28347400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr10:28344600-28348200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr10:28344600-28348400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:28344600-28348400	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr10:28344600-28348600	Weak transcription	Osteobl	bone
25	chr10:28344600-28364400	Weak transcription	Fetal Heart	heart
26	chr10:28344800-28346600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:28344800-28347000	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr10:28344800-28347600	Strong transcription	Skeletal Muscle Female	skeletal muscle
29	chr10:28345000-28346400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr10:28345000-28346800	Strong transcription	Aorta	Aorta
31	chr10:28345000-28347000	Strong transcription	Esophagus	oesophagus
32	chr10:28345000-28347000	Strong transcription	Fetal Stomach	stomach
33	chr10:28345000-28347000	Strong transcription	Left Ventricle	heart
34	chr10:28345000-28347200	Strong transcription	Stomach Smooth Muscle	stomach
35	chr10:28345000-28347600	Strong transcription	Primary B cells from cord blood	blood
36	chr10:28345000-28348200	Strong transcription	Fetal Intestine Small	intestine
37	chr10:28345000-28348400	Strong transcription	Primary T cells from cord blood	blood
38	chr10:28345000-28348400	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr10:28345000-28348600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:28345000-28354000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr10:28345200-28347000	Strong transcription	Pancreas	Pancrea
42	chr10:28345400-28347400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr10:28345400-28348200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
44	chr10:28345600-28347000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr10:28345600-28347600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr10:28345600-28349600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr10:28345800-28347000	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr10:28346000-28346400	Strong transcription	Pancreatic Islets	Pancreatic Islet
49	chr10:28346000-28346600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr10:28346000-28346600	Strong transcription	HepG2	liver

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