Variant report

Variant	rs10124709
Chromosome Location	chr9:95766881-95766882
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95739140..95740868-chr9:95765712..95767872,2	MCF-7	breast:
2	chr9:95761527..95763076-chr9:95764735..95767676,2	K562	blood:
3	chr9:95764926..95767414-chr9:95782606..95784200,2	MCF-7	breast:
4	chr9:95762280..95764088-chr9:95766810..95768314,2	MCF-7	breast:
5	chr9:95764397..95768278-chr9:95771729..95773311,3	K562	blood:
6	chr9:95750713..95751415-chr9:95766501..95767049,2	MCF-7	breast:
7	chr9:95765841..95768225-chr9:95860926..95862448,2	MCF-7	breast:
8	chr9:95766059..95768538-chr9:95781716..95783313,2	MCF-7	breast:

No data

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10115063	1.00[TSI][hapmap]
rs10116009	1.00[EUR][1000 genomes]
rs10122374	1.00[EUR][1000 genomes]
rs12340110	1.00[EUR][1000 genomes]
rs12342477	1.00[EUR][1000 genomes]
rs12349817	1.00[EUR][1000 genomes]
rs12351360	1.00[EUR][1000 genomes]
rs28864474	1.00[EUR][1000 genomes]
rs73526860	1.00[EUR][1000 genomes]

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	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1054767	chr9:95738134-95875977	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95761600-95785800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr9:95761600-95785800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr9:95762000-95767800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
4	chr9:95762000-95786400	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr9:95762200-95767400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr9:95762600-95790200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:95763000-95767200	Genic enhancers	Primary T cells fromperipheralblood	blood
8	chr9:95763000-95773400	Strong transcription	Primary B cells from cord blood	blood
9	chr9:95763600-95787200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr9:95763800-95767400	Genic enhancers	Primary T cells from cord blood	blood
11	chr9:95763800-95789400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr9:95764000-95767000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr9:95764000-95773000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:95764000-95777000	Strong transcription	Dnd41	blood
15	chr9:95764400-95768200	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr9:95764400-95774000	Strong transcription	Thymus	Thymus
17	chr9:95764600-95767200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr9:95765000-95767200	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr9:95765200-95767000	Genic enhancers	Fetal Thymus	thymus
20	chr9:95765800-95767200	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr9:95765800-95768400	Strong transcription	Brain Germinal Matrix	brain
22	chr9:95766000-95767000	Enhancers	Fetal Muscle Trunk	muscle
23	chr9:95766000-95767200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:95766000-95771200	Strong transcription	GM12878-XiMat	blood
25	chr9:95766000-95772200	Strong transcription	Primary hematopoietic stem cells	blood
26	chr9:95766200-95767000	Active TSS	Hela-S3	cervix
27	chr9:95766200-95767200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr9:95766200-95768000	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr9:95766200-95768400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
30	chr9:95766400-95767200	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr9:95766400-95767400	Strong transcription	Fetal Brain Female	brain
32	chr9:95766400-95771800	Weak transcription	Esophagus	oesophagus
33	chr9:95766400-95785600	Strong transcription	Primary B cells from peripheral blood	blood
34	chr9:95766600-95767000	Enhancers	Ovary	ovary
35	chr9:95766600-95767200	Genic enhancers	Pancreas	Pancrea
36	chr9:95766600-95767200	Genic enhancers	Spleen	Spleen
37	chr9:95766600-95767400	Strong transcription	Lung	lung
38	chr9:95766600-95767400	Enhancers	HepG2	liver
39	chr9:95766600-95767600	Strong transcription	Fetal Intestine Small	intestine
40	chr9:95766600-95769800	Weak transcription	Left Ventricle	heart
41	chr9:95766600-95770000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr9:95766600-95772600	Weak transcription	Fetal Stomach	stomach
43	chr9:95766600-95773200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:95766600-95773800	Strong transcription	Fetal Intestine Large	intestine
45	chr9:95766600-95776200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:95766600-95778000	Weak transcription	Gastric	stomach
47	chr9:95766600-95780200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:95766600-95783400	Weak transcription	Placenta	Placenta
49	chr9:95766600-95790400	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr9:95766600-95790800	Weak transcription	Right Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links