Variant report

Variant	rs10125084
Chromosome Location	chr9:970151-970152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:968342..970313-chr9:973554..975096,2	K562	blood:
2	chr9:962191..965396-chr9:970150..972525,3	MCF-7	breast:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10114780	1.00[AMR][1000 genomes]
rs10217745	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10977756	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10977854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12340459	1.00[AMR][1000 genomes]
rs12343361	1.00[AMR][1000 genomes]
rs12350113	1.00[AMR][1000 genomes]
rs28453929	1.00[AMR][1000 genomes]
rs28709376	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59635744	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9886854	1.00[AMR][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	nsv1025492	chr9:478813-1157169	Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv539897	chr9:478813-1157169	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv429977	chr9:584087-983301	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv613037	chr9:643453-1138368	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv892000	chr9:678951-972476	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv817248	chr9:706283-1457665	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv831491	chr9:794113-974142	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv892010	chr9:841152-1069663	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1034070	chr9:911265-1152351	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	esv2755928	chr9:924525-985979	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv892013	chr9:943611-1047343	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv1018926	chr9:965006-1014141	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:969200-971800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
2	chr9:969400-970400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr9:969400-971000	Enhancers	Gastric	stomach
4	chr9:969400-971200	Bivalent Enhancer	Fetal Heart	heart
5	chr9:969400-971400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr9:969400-972000	Bivalent Enhancer	Left Ventricle	heart
7	chr9:969400-972200	Bivalent Enhancer	Spleen	Spleen
8	chr9:969400-973200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
9	chr9:969400-973400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr9:969600-970200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr9:969600-970400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
12	chr9:969600-970600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
13	chr9:969600-970600	Bivalent Enhancer	Stomach Mucosa	stomach
14	chr9:969600-970800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:969600-971000	Bivalent Enhancer	Adipose Nuclei	Adipose
16	chr9:969600-971200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:969600-971200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr9:969600-971400	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr9:969600-971600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
20	chr9:969600-971600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:969600-971600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
22	chr9:969600-972000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr9:969600-972000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr9:969600-972000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:969600-972000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:969600-972000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
27	chr9:969600-973200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
28	chr9:969600-973400	Bivalent Enhancer	Lung	lung
29	chr9:969800-970200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr9:969800-970200	Bivalent Enhancer	Liver	Liver
31	chr9:969800-970600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:969800-970600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr9:969800-970600	Bivalent Enhancer	Brain Anterior Caudate	brain
34	chr9:969800-970800	Bivalent Enhancer	Brain Germinal Matrix	brain
35	chr9:969800-971400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
36	chr9:969800-971400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
37	chr9:969800-971600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr9:969800-971600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
39	chr9:969800-971600	Enhancers	Pancreas	Pancrea
40	chr9:969800-971800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
41	chr9:969800-971800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
42	chr9:969800-972000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr9:969800-972000	Bivalent Enhancer	Fetal Stomach	stomach
44	chr9:969800-972400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr9:969800-973200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr9:969800-973200	Bivalent Enhancer	Fetal Lung	lung
47	chr9:970000-970200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:970000-970200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
49	chr9:970000-970200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:970000-970400	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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